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: 0.01 (G)
Location

Chromosome 11:114059316 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.114059316T>G

Variation displays