Original source

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

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

Chromosome 2:209100758 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.209100758C>A

Variation displays