Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.27 (C)
Location

Chromosome 4:6293966 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs56732551

This variation has 5 HGVS names - click the plus to show

4:g.6293966C>G
ENST00000507765.1:n.898-1075C>G
ENST00000503569.2:c.713-1075C>G
ENST00000506362.1:c.310-1039C>G
ENST00000226760.2:c.713-1075C>G

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays