Original source

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

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

Chromosome 16:57541217 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.57541217C>A

Variation displays