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 14:23433656 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM962617 ; PhenCode FHC0099 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_004566

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts, has 2504 individual genotypes and is associated with 2 phenotypes.

Variation displays