Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.09 (A)
Location

Chromosome 1:77088956 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61049259

HGVS name

1:g.77088956G>A

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 3 transcripts and has 3681 sample genotypes.

Variant displays