Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.49 (A)

Chromosome 11:108253572 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2543 individual genotypes.

Variation displays