Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.02 (T)
Location

Chromosome 2:192748268 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.192748268G>T

Variation displays