Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.25 (A)
Location

Chromosome 3:7155702 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58347963

This variation has 12 HGVS names - click the plus to show

3:g.7155702T>A
ENST00000402647.2:c.520-32437T>A
ENST00000486284.1:c.520-32437T>A
ENST00000448328.2:c.-105-32437T>A
ENST00000389335.3:c.520-32437T>A
ENST00000443259.1:c.*116-32437T>A
ENST00000467425.1:c.520-32437T>A
ENST00000389336.4:c.520-32437T>A
ENST00000435689.1:c.75-32437T>A
ENST00000357716.4:c.520-32437T>A
ENST00000440923.3:c.520-32437T>A
ENST00000403881.1:c.520-32437T>A

Genotyping chips

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

Variation displays