Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)

Chromosome 10:74111964 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


Uniprot VAR_035102

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, has 2576 sample genotypes and is associated with 1 phenotype.

Variant displays