Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 2:119605317 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.119605317T>G

Variation displays