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rs771562210

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771562210(C;T)
Make rs771562210(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178630240
GeneTTN
is asnp
is mentioned by
dbSNPrs771562210
ebirs771562210
HLIrs771562210
Exacrs771562210
Varsomers771562210
Maprs771562210
PheGenIrs771562210
hapmaprs771562210
1000 genomesrs771562210
hgdprs771562210
ensemblrs771562210
gopubmedrs771562210
geneviewrs771562210
scholarrs771562210
googlers771562210
pharmgkbrs771562210
gwascentralrs771562210
openSNPrs771562210
23andMers771562210
23andMe allrs771562210
SNP Nexus

SNPshotrs771562210
SNPdbers771562210
MSV3drs771562210
GWAS Ctlgrs771562210
Max Magnitude0
ClinVar
Risk rs771562210(T;T)
Alt rs771562210(T;T)
Reference rs771562210(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179494967C>T
CLNSRC
CLNACC RCV000209118.1,