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rs730881102

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881102(A;A)
Make rs730881102(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201364314
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881102
ebirs730881102
HLIrs730881102
Exacrs730881102
Varsomers730881102
Maprs730881102
PheGenIrs730881102
hapmaprs730881102
1000 genomesrs730881102
hgdprs730881102
ensemblrs730881102
gopubmedrs730881102
geneviewrs730881102
scholarrs730881102
googlers730881102
pharmgkbrs730881102
gwascentralrs730881102
openSNPrs730881102
23andMers730881102
23andMe allrs730881102
SNP Nexus

SNPshotrs730881102
SNPdbers730881102
MSV3drs730881102
GWAS Ctlgrs730881102
Max Magnitude0
ClinVar
Risk rs730881102(A;A)
Alt rs730881102(A;A)
Reference rs730881102(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201333442C>T
CLNSRC
CLNACC RCV000159298.2,