Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 11:72004078 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_051248

HGVS names

This variant has 17 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 25 transcripts and has 435 sample genotypes.

Variant displays