Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.23 (A)
Location

Chromosome 1:77088768 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60962074, rs74225868

HGVS name

1:g.77088768G>A

About this variant

This variant overlaps 3 transcripts and has 2774 individual genotypes.

Variation displays