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rs606231469

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231469(A;A)
Make rs606231469(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position74369495
GeneFPGT-TNNI3K, TNNI3K
is asnp
is mentioned by
dbSNPrs606231469
ebirs606231469
HLIrs606231469
Exacrs606231469
Varsomers606231469
Maprs606231469
PheGenIrs606231469
hapmaprs606231469
1000 genomesrs606231469
hgdprs606231469
ensemblrs606231469
gopubmedrs606231469
geneviewrs606231469
scholarrs606231469
googlers606231469
pharmgkbrs606231469
gwascentralrs606231469
openSNPrs606231469
23andMers606231469
23andMe allrs606231469
SNP Nexus

SNPshotrs606231469
SNPdbers606231469
MSV3drs606231469
GWAS Ctlgrs606231469
Max Magnitude0
ClinVar
Risk rs606231469(A;A)
Alt rs606231469(A;A)
Reference rs606231469(G;G)
Significance Pathogenic
Disease Cardiac conduction disease with or without dilated cardiomyopathy
Variation info
Gene TNNI3K FPGT-TNNI3K
CLNDBN Cardiac conduction disease with or without dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.74835179G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000148950.4,