Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 2:113587321 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.113587321A>G

Variation displays