Original source

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

T/A/C | Ancestral: T | Ambiguity code: H | MAF: 0.27 (C)

Chromosome 11:1995432 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 36 transcripts, has 2573 sample genotypes and is mentioned in 2 citations.

Variant displays