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rs730881121

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881121(C;T)
Make rs730881121(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201365635
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881121
ebirs730881121
HLIrs730881121
Exacrs730881121
Varsomers730881121
Maprs730881121
PheGenIrs730881121
hapmaprs730881121
1000 genomesrs730881121
hgdprs730881121
ensemblrs730881121
gopubmedrs730881121
geneviewrs730881121
scholarrs730881121
googlers730881121
pharmgkbrs730881121
gwascentralrs730881121
openSNPrs730881121
23andMers730881121
23andMe allrs730881121
SNP Nexus

SNPshotrs730881121
SNPdbers730881121
MSV3drs730881121
GWAS Ctlgrs730881121
Max Magnitude0
ClinVar
Risk rs730881121(T;T)
Alt rs730881121(T;T)
Reference rs730881121(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201334763G>A
CLNSRC
CLNACC RCV000159336.1,