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rs111377893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111377893(C;G)
Make rs111377893(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position201359622
GeneTNNT2
is asnp
is mentioned by
dbSNPrs111377893
ebirs111377893
HLIrs111377893
Exacrs111377893
Varsomers111377893
Maprs111377893
PheGenIrs111377893
hapmaprs111377893
1000 genomesrs111377893
hgdprs111377893
ensemblrs111377893
gopubmedrs111377893
geneviewrs111377893
scholarrs111377893
googlers111377893
pharmgkbrs111377893
gwascentralrs111377893
openSNPrs111377893
23andMers111377893
23andMe allrs111377893
SNP Nexus

SNPshotrs111377893
SNPdbers111377893
MSV3drs111377893
GWAS Ctlgrs111377893
Max Magnitude0
ClinVar
Risk rs111377893(A,G,T;A,G,T)
Alt rs111377893(A,G,T;A,G,T)
Reference rs111377893(C;C)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy Cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Primary familial hypertrophic cardiomyopathy Cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.201328750C>A; NC_000001.10:g.201328750C>G; NC_000001.10:g.201328750C>T
CLNSRC ClinVar
CLNACC RCV000152095.2, RCV000159346.1, RCV000036621.3,