Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.08 (T)
Location

Chromosome 11:44095859 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

Variation displays