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rs730881100

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881100(A;A)
Make rs730881100(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201364375
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881100
ClinGenrs730881100
ebirs730881100
HLIrs730881100
Exacrs730881100
Varsomers730881100
Maprs730881100
PheGenIrs730881100
hapmaprs730881100
1000 genomesrs730881100
hgdprs730881100
ensemblrs730881100
gopubmedrs730881100
geneviewrs730881100
scholarrs730881100
googlers730881100
pharmgkbrs730881100
gwascentralrs730881100
openSNPrs730881100
23andMers730881100
23andMe allrs730881100
SNP Nexus

SNPshotrs730881100
SNPdbers730881100
MSV3drs730881100
GWAS Ctlgrs730881100
Max Magnitude0
ClinVar
Risk rs730881100(A;A)
Alt rs730881100(A;A)
Reference Rs730881100(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201333503C>T
CLNSRC
CLNACC RCV000159289.1,