Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.06 (A)

Chromosome 11:1995487 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 18 transcripts, has 2826 sample genotypes and is mentioned in 1 citation.

Variant displays