Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs17880098, rs36224103

HGVS name

11:g.34437971T>C

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2506 individual genotypes.

Variation displays