Original source

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

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

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

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

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