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 | MAF: 0.05 (G)
Location

Chromosome 11:116835452 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17249449

HGVS name

11:g.116835452T>G

Variation displays