rs1947012 - SNP

Select item 19470121.

rs1947012 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 13:19006832 (GRCh38)
13:19580972 (GRCh37)
Canonical SPDI:: NC_000013.11:19006831:C:G
Gene:: LINC00442 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.35172/6644 (ALFA)
C=0.102804/22 (Vietnamese)
C=0.105421/1767 (TOMMO)
C=0.128669/377 (KOREAN)
C=0.12963/7 (Siberian)
C=0.189189/98 (SGDP_PRJ)
C=0.269831/1351 (1000Genomes)
C=0.289634/95 (HapMap)
G=0.3/6 (PRJEB36033)
C=0.312932/82830 (TOPMED)
C=0.330962/46334 (GnomAD)
C=0.356667/214 (NorthernSweden)
C=0.369196/1654 (Estonian)
C=0.374157/1442 (ALSPAC)
C=0.377292/1399 (TWINSUK)
C=0.4/16 (GENOME_DK)
C=0.423848/423 (GoNL)
C=0.476852/103 (Qatari)
HGVS:: NC_000013.11:g.19006832C>G, NC_000013.10:g.19580972C>G

Select item 594262712.

rs59426271 has merged into rs1947012 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 13:19006832 (GRCh38)
13:19580972 (GRCh37)
Canonical SPDI:: NC_000013.11:19006831:C:G
Gene:: LINC00442 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.35172/6644 (ALFA)
C=0.102804/22 (Vietnamese)
C=0.105421/1767 (TOMMO)
C=0.128669/377 (KOREAN)
C=0.12963/7 (Siberian)
C=0.189189/98 (SGDP_PRJ)
C=0.269831/1351 (1000Genomes)
C=0.289634/95 (HapMap)
G=0.3/6 (PRJEB36033)
C=0.312932/82830 (TOPMED)
C=0.330962/46334 (GnomAD)
C=0.356667/214 (NorthernSweden)
C=0.369196/1654 (Estonian)
C=0.374157/1442 (ALSPAC)
C=0.377292/1399 (TWINSUK)
C=0.4/16 (GENOME_DK)
C=0.423848/423 (GoNL)
C=0.476852/103 (Qatari)
HGVS:: NC_000013.11:g.19006832C>G, NC_000013.10:g.19580972C>G

Select item 46240103.

rs4624010 has merged into rs1947012 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 13:19006832 (GRCh38)
13:19580972 (GRCh37)
Canonical SPDI:: NC_000013.11:19006831:C:G
Gene:: LINC00442 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.35172/6644 (ALFA)
C=0.102804/22 (Vietnamese)
C=0.105421/1767 (TOMMO)
C=0.128669/377 (KOREAN)
C=0.12963/7 (Siberian)
C=0.189189/98 (SGDP_PRJ)
C=0.269831/1351 (1000Genomes)
C=0.289634/95 (HapMap)
G=0.3/6 (PRJEB36033)
C=0.312932/82830 (TOPMED)
C=0.330962/46334 (GnomAD)
C=0.356667/214 (NorthernSweden)
C=0.369196/1654 (Estonian)
C=0.374157/1442 (ALSPAC)
C=0.377292/1399 (TWINSUK)
C=0.4/16 (GENOME_DK)
C=0.423848/423 (GoNL)
C=0.476852/103 (Qatari)
HGVS:: NC_000013.11:g.19006832C>G, NC_000013.10:g.19580972C>G

dbSNP