Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.46 (T)
Location

Chromosome 11:46087968 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2509 individual genotypes.

Variation displays