Original source

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

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

Chromosome 10:74070769 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 2545 sample genotypes and is associated with 2 phenotypes.

Variant displays