SNP - NCBI

Format

Choose Destination

Select item 88961.

rs8896 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:633438 (GRCh38)
1:568818 (GRCh37)
Canonical SPDI:: NC_000001.11:633437:G:A
Gene:: MIR12136 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00674/110 (ALFA)
A=0.00015/11 (TOMMO)
A=0.0012/6 (1000Genomes)
G=0.5/2 (SGDP_PRJ)
HGVS:: NC_000001.11:g.633438G>A, NC_000001.10:g.568818G>A, NG_046448.1:g.782G>A, NG_045722.1:g.4G>A, NM_173705.1:c.684G>A

Supplemental Content

dbSNP