Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_035102

This variation has 11 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 7 transcripts, has 2531 individual genotypes and is associated with 1 phenotype.

Variation displays