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 17:18449838 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs2621709

HGVS name

17:g.18449838C>A

Variation displays