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rs730882252

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730882252(A;G)
Make rs730882252(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position90404482
GeneCALM1
is asnp
is mentioned by
dbSNPrs730882252
ebirs730882252
HLIrs730882252
Exacrs730882252
Varsomers730882252
Maprs730882252
PheGenIrs730882252
hapmaprs730882252
1000 genomesrs730882252
hgdprs730882252
ensemblrs730882252
gopubmedrs730882252
geneviewrs730882252
scholarrs730882252
googlers730882252
pharmgkbrs730882252
gwascentralrs730882252
openSNPrs730882252
23andMers730882252
23andMe allrs730882252
SNP Nexus

SNPshotrs730882252
SNPdbers730882252
MSV3drs730882252
GWAS Ctlgrs730882252
Max Magnitude0
ClinVar
Risk rs730882252(G;G)
Alt rs730882252(G;G)
Reference rs730882252(A;A)
Significance Pathogenic
Disease Long QT syndrome 14
Variation info
Gene CALM1
CLNDBN Long QT syndrome 14
Reversed 0
HGVS NC_000014.8:g.90870826A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000162062.2,