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rs730881114

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881114(G;T)
Make rs730881114(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201359256
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881114
ebirs730881114
HLIrs730881114
Exacrs730881114
Varsomers730881114
Maprs730881114
PheGenIrs730881114
hapmaprs730881114
1000 genomesrs730881114
hgdprs730881114
ensemblrs730881114
gopubmedrs730881114
geneviewrs730881114
scholarrs730881114
googlers730881114
pharmgkbrs730881114
gwascentralrs730881114
openSNPrs730881114
23andMers730881114
23andMe allrs730881114
SNP Nexus

SNPshotrs730881114
SNPdbers730881114
MSV3drs730881114
GWAS Ctlgrs730881114
Max Magnitude0
ClinVar
Risk rs730881114(T;T)
Alt rs730881114(T;T)
Reference rs730881114(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201328384C>A
CLNSRC
CLNACC RCV000159320.2,