Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.08 (A)

Chromosome 10:69268902 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2505 sample genotypes.

Variant displays