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rs727503513

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503513(C;T)
Make rs727503513(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201365292
GeneTNNT2
is asnp
is mentioned by
dbSNPrs727503513
ebirs727503513
HLIrs727503513
Exacrs727503513
Varsomers727503513
Maprs727503513
PheGenIrs727503513
hapmaprs727503513
1000 genomesrs727503513
hgdprs727503513
ensemblrs727503513
gopubmedrs727503513
geneviewrs727503513
scholarrs727503513
googlers727503513
pharmgkbrs727503513
gwascentralrs727503513
openSNPrs727503513
23andMers727503513
23andMe allrs727503513
SNP Nexus

SNPshotrs727503513
SNPdbers727503513
MSV3drs727503513
GWAS Ctlgrs727503513
Max Magnitude0
ClinVar
Risk rs727503513(T;T)
Alt rs727503513(T;T)
Reference rs727503513(C;C)
Significance Other
Disease Familial restrictive cardiomyopathy not provided
Variation info
Gene TNNT2
CLNDBN Familial restrictive cardiomyopathy not provided
Reversed 1
HGVS NC_000001.10:g.201334420G>A
CLNSRC
CLNACC RCV000152104.1, RCV000159282.2,