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rs730880059

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880059(A;A)
Make rs730880059(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position18539383
GeneCACNB2, LOC105376439
is asnp
is mentioned by
dbSNPrs730880059
ebirs730880059
HLIrs730880059
Exacrs730880059
Varsomers730880059
Maprs730880059
PheGenIrs730880059
hapmaprs730880059
1000 genomesrs730880059
hgdprs730880059
ensemblrs730880059
gopubmedrs730880059
geneviewrs730880059
scholarrs730880059
googlers730880059
pharmgkbrs730880059
gwascentralrs730880059
openSNPrs730880059
23andMers730880059
23andMe allrs730880059
SNP Nexus

SNPshotrs730880059
SNPdbers730880059
MSV3drs730880059
GWAS Ctlgrs730880059
Max Magnitude0
ClinVar
Risk rs730880059(A;A)
Alt rs730880059(A;A)
Reference rs730880059(G;G)
Significance Probable-Pathogenic
Disease Cardiac arrest not provided
Variation info
Gene CACNB2
CLNDBN Cardiac arrest not provided
Reversed 0
HGVS NC_000010.10:g.18828312G>A
CLNSRC
CLNACC RCV000157131.1, RCV000170873.2,