Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.16 (A)

Chromosome 10:87863959 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2593 sample genotypes and is mentioned in 3 citations.

Variant displays