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rs730881103

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881103(C;G)
Make rs730881103(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201363394
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881103
ebirs730881103
HLIrs730881103
Exacrs730881103
Varsomers730881103
Maprs730881103
PheGenIrs730881103
hapmaprs730881103
1000 genomesrs730881103
hgdprs730881103
ensemblrs730881103
gopubmedrs730881103
geneviewrs730881103
scholarrs730881103
googlers730881103
pharmgkbrs730881103
gwascentralrs730881103
openSNPrs730881103
23andMers730881103
23andMe allrs730881103
SNP Nexus

SNPshotrs730881103
SNPdbers730881103
MSV3drs730881103
GWAS Ctlgrs730881103
Max Magnitude0
ClinVar
Risk rs730881103(G,T;G,T)
Alt rs730881103(G,T;G,T)
Reference rs730881103(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201332522G>C
CLNSRC
CLNACC RCV000159300.2,