Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.35 (G)
Location

Chromosome 3:7477085 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 11 HGVS names - Hide

3:g.7477085A>G
ENST00000402647.6:c.780+15363A>G
ENST00000486284.5:c.1515+15363A>G
ENST00000445087.1:c.486+15363A>G
ENST00000389335.7:c.1515+15363A>G
ENST00000389336.8:c.1515+15363A>G
ENST00000467425.5:c.1515+15363A>G
ENST00000463676.6:n.780+15363A>G
ENST00000458641.2:n.380+15363A>G
ENST00000357716.8:c.1515+15363A>G
ENST00000440923.7:c.1515+15363A>G

Genotyping chips

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

About this variant

This variant overlaps 10 transcripts, has 3968 sample genotypes and is mentioned in 3 citations.

Variant displays