Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.17 (A)

Chromosome 7:94627959 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59328897

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2903 sample genotypes.

Variant displays