Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.07 (A)
Location

Chromosome 11:101583461 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 2505 sample genotypes and is mentioned in 4 citations.

Variant displays