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 3:38697563 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

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

Variation displays