Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.16 (C)
Location

Chromosome 1:20650872 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3795511, rs3182991

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts, has 2512 sample genotypes and is mentioned in 1 citation.

Variant displays