Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.24 (G)

Chromosome 11:113475096 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2508 sample genotypes.

Variant displays