Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.34 (G)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61034247, rs3804955

This variation has 11 HGVS names - click the plus to show

3:g.7477085A>G
ENST00000402647.5:c.780+15363A>G
ENST00000486284.4:c.1515+15363A>G
ENST00000445087.1:c.486+15363A>G
ENST00000389335.6:c.1515+15363A>G
ENST00000467425.4:c.1515+15363A>G
ENST00000389336.7:c.1515+15363A>G
ENST00000463676.5:n.780+15363A>G
ENST00000458641.2:n.380+15363A>G
ENST00000357716.7:c.1515+15363A>G
ENST00000440923.6:c.1515+15363A>G

Genotyping chips

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

About this variant

This variant overlaps 10 transcripts, has 2568 individual genotypes and is mentioned in 3 citations.

Variation displays