Original source

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

Alleles
G/C|Ancestral: C|Ambiguity code: S|MAF: 0.43 (C)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3804948, rs60436138

HGVS names

This variant has 11 HGVS names - Hide

3:g.7482355G>C
ENST00000402647.6:c.780+20633G>C
ENST00000486284.5:c.1515+20633G>C
ENST00000445087.1:c.486+20633G>C
ENST00000389335.7:c.1515+20633G>C
ENST00000463676.6:n.780+20633G>C
ENST00000467425.5:c.1515+20633G>C
ENST00000389336.8:c.1515+20633G>C
ENST00000458641.2:n.380+20633G>C
ENST00000357716.8:c.1515+20633G>C
ENST00000440923.7:c.1515+20633G>C

Genotyping chips

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

About this variant

This variant overlaps 10 transcripts, has 6010 sample genotypes and is mentioned in 1 citation.

Variant displays