Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.31 (C)
Location

Chromosome 8:31067041 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

This variant has 5 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 3384 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays