Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/- | Ancestral: C | MAF: 0.16 (-)
Location

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

Co-located

with dbSNP rs76969449 (C/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs148036771

HGVS name

17:g.58169015delC

About this variant

This variant overlaps 1 transcript and has 1095 individual genotypes.

Variation displays