Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.31 (A)
Location

Chromosome 8:63080488 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs7817047, rs58939252

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2506 individual genotypes.

Variation displays