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rs730881112

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881112(C;C)
Make rs730881112(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201361284
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881112
ebirs730881112
HLIrs730881112
Exacrs730881112
Varsomers730881112
Maprs730881112
PheGenIrs730881112
hapmaprs730881112
1000 genomesrs730881112
hgdprs730881112
ensemblrs730881112
gopubmedrs730881112
geneviewrs730881112
scholarrs730881112
googlers730881112
pharmgkbrs730881112
gwascentralrs730881112
openSNPrs730881112
23andMers730881112
23andMe allrs730881112
SNP Nexus

SNPshotrs730881112
SNPdbers730881112
MSV3drs730881112
GWAS Ctlgrs730881112
Max Magnitude0
ClinVar
Risk rs730881112(C;C)
Alt rs730881112(C;C)
Reference rs730881112(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201330412A>G
CLNSRC
CLNACC RCV000159317.2,