rs235858 - SNP

Select item 2358581.

rs235858 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:171627362 (GRCh38)
1:171596502 (GRCh37)
Canonical SPDI:: NC_000001.11:171627361:G:A,NC_000001.11:171627361:G:T
Gene:: MYOCOS (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.411247/10926 (ALFA)
G=0.25/54 (Qatari)
G=0.272321/122 (SGDP_PRJ)
G=0.285714/16 (Siberian)
G=0.32386/5428 (TOMMO)
G=0.326638/618 (HapMap)
G=0.335467/46952 (GnomAD)
G=0.342231/90585 (TOPMED)
G=0.346034/1733 (1000Genomes)
G=0.372991/1671 (Estonian)
G=0.375/15 (GENOME_DK)
G=0.387909/1495 (ALSPAC)
G=0.395361/1466 (TWINSUK)
G=0.410822/410 (GoNL)
G=0.43/258 (NorthernSweden)
G=0.43286/793 (Korea1K)
G=0.43413/1272 (KOREAN)
A=0.48722/305 (Chileans)
A=0.490566/104 (Vietnamese)
HGVS:: NC_000001.11:g.171627362G>A, NC_000001.11:g.171627362G>T, NC_000001.10:g.171596502G>A, NC_000001.10:g.171596502G>T

Select item 8727552.

rs872755 has merged into rs235858 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:171627362 (GRCh38)
1:171596502 (GRCh37)
Canonical SPDI:: NC_000001.11:171627361:G:A,NC_000001.11:171627361:G:T
Gene:: MYOCOS (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.411247/10926 (ALFA)
G=0.25/54 (Qatari)
G=0.272321/122 (SGDP_PRJ)
G=0.285714/16 (Siberian)
G=0.32386/5428 (TOMMO)
G=0.326638/618 (HapMap)
G=0.335467/46952 (GnomAD)
G=0.342231/90585 (TOPMED)
G=0.346034/1733 (1000Genomes)
G=0.372991/1671 (Estonian)
G=0.375/15 (GENOME_DK)
G=0.387909/1495 (ALSPAC)
G=0.395361/1466 (TWINSUK)
G=0.410822/410 (GoNL)
G=0.43/258 (NorthernSweden)
G=0.43286/793 (Korea1K)
G=0.43413/1272 (KOREAN)
A=0.48722/305 (Chileans)
A=0.490566/104 (Vietnamese)
HGVS:: NC_000001.11:g.171627362G>A, NC_000001.11:g.171627362G>T, NC_000001.10:g.171596502G>A, NC_000001.10:g.171596502G>T

Select item 5788923.

rs578892 has merged into rs235858 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:171627362 (GRCh38)
1:171596502 (GRCh37)
Canonical SPDI:: NC_000001.11:171627361:G:A,NC_000001.11:171627361:G:T
Gene:: MYOCOS (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.411247/10926 (ALFA)
G=0.25/54 (Qatari)
G=0.272321/122 (SGDP_PRJ)
G=0.285714/16 (Siberian)
G=0.32386/5428 (TOMMO)
G=0.326638/618 (HapMap)
G=0.335467/46952 (GnomAD)
G=0.342231/90585 (TOPMED)
G=0.346034/1733 (1000Genomes)
G=0.372991/1671 (Estonian)
G=0.375/15 (GENOME_DK)
G=0.387909/1495 (ALSPAC)
G=0.395361/1466 (TWINSUK)
G=0.410822/410 (GoNL)
G=0.43/258 (NorthernSweden)
G=0.43286/793 (Korea1K)
G=0.43413/1272 (KOREAN)
A=0.48722/305 (Chileans)
A=0.490566/104 (Vietnamese)
HGVS:: NC_000001.11:g.171627362G>A, NC_000001.11:g.171627362G>T, NC_000001.10:g.171596502G>A, NC_000001.10:g.171596502G>T

dbSNP