Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.44 (A)

Chromosome 17:34357972 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs63170661

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, has 2510 sample genotypes and is mentioned in 1 citation.

Variant displays