Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.04 (C)
Location

Chromosome 11:34437971 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs17880098, rs36224103

HGVS name

11:g.34437971T>C

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 1 transcript and has 2548 sample genotypes.

Variant displays