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rs148515772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148515772(A;A)
Make rs148515772(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154380902
GeneEMD
is asnp
is mentioned by
dbSNPrs148515772
ebirs148515772
HLIrs148515772
Exacrs148515772
Varsomers148515772
Maprs148515772
PheGenIrs148515772
hapmaprs148515772
1000 genomesrs148515772
hgdprs148515772
ensemblrs148515772
gopubmedrs148515772
geneviewrs148515772
scholarrs148515772
googlers148515772
pharmgkbrs148515772
gwascentralrs148515772
openSNPrs148515772
23andMers148515772
23andMe allrs148515772
SNP Nexus

SNPshotrs148515772
SNPdbers148515772
MSV3drs148515772
GWAS Ctlgrs148515772
Max Magnitude0
ClinVar
Risk rs148515772(A;A)
Alt rs148515772(A;A)
Reference rs148515772(G;G)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene EMD
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000023.10:g.153609262G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029690.1,