Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.41 (C)
Location

Chromosome 3:7482355 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3804948, rs60436138

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

3:g.7482355G>C
ENST00000402647.3:c.891+20633G>C
ENST00000486284.2:c.1515+20633G>C
ENST00000445087.1:c.486+20633G>C
ENST00000389335.4:c.1515+20633G>C
ENST00000467425.2:c.1515+20633G>C
ENST00000389336.5:c.1515+20633G>C
ENST00000463676.3:n.780+20633G>C
ENST00000458641.2:n.380+20633G>C
ENST00000357716.5:c.1515+20633G>C
ENST00000440923.4:c.1515+20633G>C

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1

Variation displays