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rs730881097

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881097(G;T)
Make rs730881097(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201363352
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881097
ebirs730881097
HLIrs730881097
Exacrs730881097
Varsomers730881097
Maprs730881097
PheGenIrs730881097
hapmaprs730881097
1000 genomesrs730881097
hgdprs730881097
ensemblrs730881097
gopubmedrs730881097
geneviewrs730881097
scholarrs730881097
googlers730881097
pharmgkbrs730881097
gwascentralrs730881097
openSNPrs730881097
23andMers730881097
23andMe allrs730881097
SNP Nexus

SNPshotrs730881097
SNPdbers730881097
MSV3drs730881097
GWAS Ctlgrs730881097
Max Magnitude0
ClinVar
Risk rs730881097(T;T)
Alt rs730881097(T;T)
Reference rs730881097(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201332480C>A
CLNSRC
CLNACC RCV000159276.2,