Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 10:71617355 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM050545

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_024030

This variation has 19 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts, has 2504 individual genotypes and is associated with 1 phenotype.

Variation displays