Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.10 (T)

Chromosome 11:117661016 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57276883, rs56525925

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3967 sample genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variant displays