Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.30 (G)
Location

Chromosome 9:99146083 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 6 transcripts, has 4162 sample genotypes, is associated with 2 phenotypes and is mentioned in 3 citations.

Variant displays