Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.20 (T)

Chromosome 11:2303462 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and has 2511 sample genotypes.

Variant displays