Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: < 0.01 (C)
Location

Chromosome 2:56092702 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.56092702A>C

Variation displays