Original source

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

Alleles
T/A|Ancestral: A|Ambiguity code: W|MAF: 0.26 (A)
Location

Chromosome 3:7114015 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58347963

HGVS names

This variant has 10 HGVS names - Hide

3:g.7114015T>A
ENST00000486284.5:c.520-32437T>A
ENST00000448328.6:c.-105-32437T>A
ENST00000443259.1:c.*116-32437T>A
ENST00000389335.7:c.520-32437T>A
ENST00000467425.5:c.520-32437T>A
ENST00000389336.8:c.520-32437T>A
ENST00000435689.5:c.75-32437T>A
ENST00000357716.8:c.520-32437T>A
ENST00000440923.7:c.520-32437T>A

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 9 transcripts, has 3972 sample genotypes and is mentioned in 5 citations.

Variant displays