Original source

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

Alleles
C/-|Ancestral: C|MAF: 0.17 (-)
Location

Chromosome 17:58169015 (forward strand)|View in location tab

Co-located variant

dbSNP rs76969449 (C/G)

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs148036771

HGVS name

17:g.58169015delC

About this variant

This variant overlaps 1 transcript and has 2507 sample genotypes.

Variant displays