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rs869312102

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312102(A;A)
Make rs869312102(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178741321
GeneTTN
is asnp
is mentioned by
dbSNPrs869312102
ebirs869312102
HLIrs869312102
Exacrs869312102
Varsomers869312102
Maprs869312102
PheGenIrs869312102
hapmaprs869312102
1000 genomesrs869312102
hgdprs869312102
ensemblrs869312102
gopubmedrs869312102
geneviewrs869312102
scholarrs869312102
googlers869312102
pharmgkbrs869312102
gwascentralrs869312102
openSNPrs869312102
23andMers869312102
23andMe allrs869312102
SNP Nexus

SNPshotrs869312102
SNPdbers869312102
MSV3drs869312102
GWAS Ctlgrs869312102
Max Magnitude0
ClinVar
Risk rs869312102(A;A)
Alt rs869312102(A;A)
Reference rs869312102(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179606048C>T
CLNSRC
CLNACC RCV000209746.1,