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rs730881096

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881096(A;A)
Make rs730881096(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201365645
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881096
ebirs730881096
HLIrs730881096
Exacrs730881096
Varsomers730881096
Maprs730881096
PheGenIrs730881096
hapmaprs730881096
1000 genomesrs730881096
hgdprs730881096
ensemblrs730881096
gopubmedrs730881096
geneviewrs730881096
scholarrs730881096
googlers730881096
pharmgkbrs730881096
gwascentralrs730881096
openSNPrs730881096
23andMers730881096
23andMe allrs730881096
SNP Nexus

SNPshotrs730881096
SNPdbers730881096
MSV3drs730881096
GWAS Ctlgrs730881096
Max Magnitude0
ClinVar
Risk rs730881096(A;A)
Alt rs730881096(A;A)
Reference rs730881096(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201334773G>T
CLNSRC
CLNACC RCV000159271.1,