Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.14 (A)
Location

Chromosome 10:98367794 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs56495379, rs61199351

HGVS name

10:g.98367794G>A

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant has 4307 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays