Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 2:118847749 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.118847749T>G

Variation displays