Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.03 (A)
Location

Chromosome 7:2538326 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_061594

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

Variant displays