rs9341266 - SNP

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Select item 93412661.

rs9341266 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:38068851 (GRCh38)
2:38295994 (GRCh37)
Canonical SPDI:: NC_000002.12:38068850:G:A
Gene:: CYP1B1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.045316/11415 (ALFA)
A=0.025/1 (GENOME_DK)
A=0.026278/2068 (PAGE_STUDY)
A=0.03455/9145 (TOPMED)
A=0.036705/5143 (GnomAD)
A=0.037946/170 (Estonian)
A=0.038076/38 (GoNL)
A=0.038296/142 (TWINSUK)
A=0.040393/74 (Korea1K)
A=0.042182/75 (HapMap)
A=0.043103/722 (TOMMO)
A=0.045859/134 (KOREAN)
A=0.046296/10 (Qatari)
A=0.046729/10 (Vietnamese)
A=0.048521/187 (ALSPAC)
A=0.053333/32 (NorthernSweden)
A=0.057152/286 (1000Genomes)
A=0.064557/51 (PRJEB37584)
G=0.466667/28 (SGDP_PRJ)
HGVS:: NC_000002.12:g.38068851G>A, NC_000002.11:g.38295994G>A, NG_008386.2:g.12251C>T, NM_000104.4:c.*1871C>T, NM_000104.3:c.*1871C>T

Select item 3866219642.

rs386621964 has merged into rs9341266 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:38068851 (GRCh38)
2:38295994 (GRCh37)
Canonical SPDI:: NC_000002.12:38068850:G:A
Gene:: CYP1B1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Clinical significance:: benign
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.045316/11415 (ALFA)
A=0.025/1 (GENOME_DK)
A=0.026278/2068 (PAGE_STUDY)
A=0.03455/9145 (TOPMED)
A=0.036705/5143 (GnomAD)
A=0.037946/170 (Estonian)
A=0.038076/38 (GoNL)
A=0.038296/142 (TWINSUK)
A=0.040393/74 (Korea1K)
A=0.042182/75 (HapMap)
A=0.043103/722 (TOMMO)
A=0.045859/134 (KOREAN)
A=0.046296/10 (Qatari)
A=0.046729/10 (Vietnamese)
A=0.048521/187 (ALSPAC)
A=0.053333/32 (NorthernSweden)
A=0.057152/286 (1000Genomes)
A=0.064557/51 (PRJEB37584)
G=0.466667/28 (SGDP_PRJ)
HGVS:: NC_000002.12:g.38068851G>A, NC_000002.11:g.38295994G>A, NG_008386.2:g.12251C>T, NM_000104.4:c.*1871C>T, NM_000104.3:c.*1871C>T