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rs193922620

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922620(A;A)
Make rs193922620(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201359618
GeneTNNT2
is asnp
is mentioned by
dbSNPrs193922620
ebirs193922620
HLIrs193922620
Exacrs193922620
Varsomers193922620
Maprs193922620
PheGenIrs193922620
hapmaprs193922620
1000 genomesrs193922620
hgdprs193922620
ensemblrs193922620
gopubmedrs193922620
geneviewrs193922620
scholarrs193922620
googlers193922620
pharmgkbrs193922620
gwascentralrs193922620
openSNPrs193922620
23andMers193922620
23andMe allrs193922620
SNP Nexus

SNPshotrs193922620
SNPdbers193922620
MSV3drs193922620
GWAS Ctlgrs193922620
Max Magnitude0
ClinVar
Risk rs193922620(A;A)
Alt rs193922620(A;A)
Reference rs193922620(G;G)
Significance Pathogenic
Disease Cardiomyopathy not provided
Variation info
Gene TNNT2
CLNDBN Cardiomyopathy not provided
Reversed 1
HGVS NC_000001.10:g.201328746C>T
CLNSRC
CLNACC RCV000030568.1, RCV000225739.1,