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rs730881116

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881116(A;A)
Make rs730881116(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201359216
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881116
ebirs730881116
HLIrs730881116
Exacrs730881116
Varsomers730881116
Maprs730881116
PheGenIrs730881116
hapmaprs730881116
1000 genomesrs730881116
hgdprs730881116
ensemblrs730881116
gopubmedrs730881116
geneviewrs730881116
scholarrs730881116
googlers730881116
pharmgkbrs730881116
gwascentralrs730881116
openSNPrs730881116
23andMers730881116
23andMe allrs730881116
SNP Nexus

SNPshotrs730881116
SNPdbers730881116
MSV3drs730881116
GWAS Ctlgrs730881116
Max Magnitude0
ClinVar
Risk rs730881116(A;A)
Alt rs730881116(A;A)
Reference rs730881116(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201328344C>T
CLNSRC
CLNACC RCV000159328.2,