Original source

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

T/A/G | Ancestral: T | Ambiguity code: D | MAF: 0.06 (G)

Chromosome 17:63918839 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs17841596

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 14 transcripts, 1 regulatory feature, has 2507 sample genotypes and is mentioned in 1 citation.

Variant displays