Original source

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

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

Chromosome 16:31178315 (forward strand) | View in location tab

Most severe consequence
HGVS name

16:g.31178315A>C

Variation displays