Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.41 (A)
Location

Chromosome 8:132865378 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR116924

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs3758115, rs61207978

HGVS name

8:g.132865378A>G

About this variant

This variant overlaps 2 transcripts, has 2775 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variant displays