Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.07 (A)
Location

Chromosome 3:129062205 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM014862

Most severe consequence
 
Missense variant
Evidence status

This variant has 2 synonyms - click the plus to show

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

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays