Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.42 (G)
Location

Chromosome 1:11021823 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 35 transcripts and has 2778 individual genotypes.

Variation displays