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

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts, has 1116 individual genotypes and is mentioned in 2 citations.

Variation displays