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rs730881115

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881115(-;-)
Make rs730881115(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201364336
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881115
ClinGenrs730881115
ebirs730881115
HLIrs730881115
Exacrs730881115
Varsomers730881115
Maprs730881115
PheGenIrs730881115
hapmaprs730881115
1000 genomesrs730881115
hgdprs730881115
ensemblrs730881115
gopubmedrs730881115
geneviewrs730881115
scholarrs730881115
googlers730881115
pharmgkbrs730881115
gwascentralrs730881115
openSNPrs730881115
23andMers730881115
23andMe allrs730881115
SNP Nexus

SNPshotrs730881115
SNPdbers730881115
MSV3drs730881115
GWAS Ctlgrs730881115
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs730881115(C;C)
Significance Probable-Pathogenic
Disease not specified Left ventricular noncompaction 6
Variation info
Gene TNNT2
CLNDBN not specified Left ventricular noncompaction 6
Reversed 1
HGVS NC_000001.10:g.201333464delG
CLNSRC
CLNACC RCV000159327.3, RCV000240641.1,