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rs45550635

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs45550635(C;C)
Make rs45550635(C;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position19192439
GeneCSRP3
is asnp
is mentioned by
dbSNPrs45550635
ebirs45550635
HLIrs45550635
Exacrs45550635
Varsomers45550635
Maprs45550635
PheGenIrs45550635
hapmaprs45550635
1000 genomesrs45550635
hgdprs45550635
ensemblrs45550635
gopubmedrs45550635
geneviewrs45550635
scholarrs45550635
googlers45550635
pharmgkbrs45550635
gwascentralrs45550635
openSNPrs45550635
23andMers45550635
23andMe allrs45550635
SNP Nexus

SNPshotrs45550635
SNPdbers45550635
MSV3drs45550635
GWAS Ctlgrs45550635
GMAF0.002755
Max Magnitude0
OMIM600824
Desc
Variant0001
Relatedalso
ClinVar
Risk rs45550635(C;C)
Alt rs45550635(C;C)
Reference rs45550635(T;T)
Significance Probable-non-pathogenic
Disease Dilated cardiomyopathy 1M not specified Dilated cardiomyopathy Cardiomyopathy Familial hypertrophic cardiomyopathy 12
Variation info
Gene CSRP3
CLNDBN Dilated cardiomyopathy 1M not specified Dilated cardiomyopathy Cardiomyopathy Familial hypertrophic cardiomyopathy 12
Reversed 1
HGVS NC_000011.9:g.19213986A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000009321.4, RCV000150371.2, RCV000172743.1, RCV000183329.1, RCV000201441.1, RCV000205519.2,