Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 16:31189636 (forward strand) | View in location tab

Most severe consequence
HGVS name

16:g.31189636A>C

Variation displays