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 16:88812533 (forward strand) | View in location tab

Most severe consequence
HGVS name

16:g.88812533C>A

Variation displays