Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 3:184375988 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 3 synonyms - click the plus to show

This variant has 8 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 16 transcripts and has 2 sample genotypes.

Variant displays