Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 17:56246376 (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.56246376delC

Variation displays