Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/A/G | Ancestral: T | Ambiguity code: D | MAF: 0.08 (A)
Location

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

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs17841596

This variant has 2 HGVS names - click the plus to show

About this variant

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

Variant displays