Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58347963

This variation has 10 HGVS names - click the plus to show

3:g.7114015T>A
ENST00000448328.5:c.-105-32437T>A
ENST00000486284.4:c.520-32437T>A
ENST00000443259.1:c.*116-32437T>A
ENST00000389335.6:c.520-32437T>A
ENST00000389336.7:c.520-32437T>A
ENST00000467425.4:c.520-32437T>A
ENST00000357716.7:c.520-32437T>A
ENST00000435689.4:c.75-32437T>A
ENST00000440923.6:c.520-32437T>A

Genotyping chips

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

About this variant

This variant overlaps 9 transcripts, has 2567 individual genotypes and is mentioned in 5 citations.

Variation displays