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rs730881104

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881104(A;G)
Make rs730881104(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201363370
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881104
ebirs730881104
HLIrs730881104
Exacrs730881104
Varsomers730881104
Maprs730881104
PheGenIrs730881104
hapmaprs730881104
1000 genomesrs730881104
hgdprs730881104
ensemblrs730881104
gopubmedrs730881104
geneviewrs730881104
scholarrs730881104
googlers730881104
pharmgkbrs730881104
gwascentralrs730881104
openSNPrs730881104
23andMers730881104
23andMe allrs730881104
SNP Nexus

SNPshotrs730881104
SNPdbers730881104
MSV3drs730881104
GWAS Ctlgrs730881104
Max Magnitude0
ClinVar
Risk rs730881104(G;G)
Alt rs730881104(G;G)
Reference rs730881104(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201332498T>C
CLNSRC
CLNACC RCV000159303.2,