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rs368180702

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368180702(C;T)
Make rs368180702(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333698
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs368180702
ebirs368180702
HLIrs368180702
Exacrs368180702
Varsomers368180702
Maprs368180702
PheGenIrs368180702
hapmaprs368180702
1000 genomesrs368180702
hgdprs368180702
ensemblrs368180702
gopubmedrs368180702
geneviewrs368180702
scholarrs368180702
googlers368180702
pharmgkbrs368180702
gwascentralrs368180702
openSNPrs368180702
23andMers368180702
23andMe allrs368180702
SNP Nexus

SNPshotrs368180702
SNPdbers368180702
MSV3drs368180702
GWAS Ctlgrs368180702
Max Magnitude0
ClinVar
Risk rs368180702(T;T)
Alt rs368180702(T;T)
Reference rs368180702(C;C)
Significance Probable-Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47355249C>T
CLNSRC
CLNACC RCV000035552.3, RCV000148672.1, RCV000227517.1,