Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.05 (-)
Location

Chromosome 16:31178121 (forward strand) | View in location tab

Co-located

with dbSNP rs12051357 (C/A/T)

Most severe consequence
HGVS name

16:g.31178121delC

Variation displays