Original source

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

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

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 2 citations.

Variant displays