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rs374615369

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374615369(C;T)
Make rs374615369(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178774305
GeneTTN
is asnp
is mentioned by
dbSNPrs374615369
ebirs374615369
HLIrs374615369
Exacrs374615369
Varsomers374615369
Maprs374615369
PheGenIrs374615369
hapmaprs374615369
1000 genomesrs374615369
hgdprs374615369
ensemblrs374615369
gopubmedrs374615369
geneviewrs374615369
scholarrs374615369
googlers374615369
pharmgkbrs374615369
gwascentralrs374615369
openSNPrs374615369
23andMers374615369
23andMe allrs374615369
SNP Nexus

SNPshotrs374615369
SNPdbers374615369
MSV3drs374615369
GWAS Ctlgrs374615369
Max Magnitude0
ClinVar
Risk rs374615369(T;T)
Alt rs374615369(T;T)
Reference rs374615369(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179639032C>T
CLNSRC
CLNACC RCV000171324.1,