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rs730881113

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881113(A;A)
Make rs730881113(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201361274
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881113
ebirs730881113
HLIrs730881113
Exacrs730881113
Varsomers730881113
Maprs730881113
PheGenIrs730881113
hapmaprs730881113
1000 genomesrs730881113
hgdprs730881113
ensemblrs730881113
gopubmedrs730881113
geneviewrs730881113
scholarrs730881113
googlers730881113
pharmgkbrs730881113
gwascentralrs730881113
openSNPrs730881113
23andMers730881113
23andMe allrs730881113
SNP Nexus

SNPshotrs730881113
SNPdbers730881113
MSV3drs730881113
GWAS Ctlgrs730881113
Max Magnitude0
ClinVar
Risk rs730881113(A,C;A,C)
Alt rs730881113(A,C;A,C)
Reference rs730881113(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201330402C>T
CLNSRC
CLNACC RCV000159318.2,