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rs368282893

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368282893(C;T)
Make rs368282893(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178782297
GeneTTN
is asnp
is mentioned by
dbSNPrs368282893
ebirs368282893
HLIrs368282893
Exacrs368282893
Varsomers368282893
Maprs368282893
PheGenIrs368282893
hapmaprs368282893
1000 genomesrs368282893
hgdprs368282893
ensemblrs368282893
gopubmedrs368282893
geneviewrs368282893
scholarrs368282893
googlers368282893
pharmgkbrs368282893
gwascentralrs368282893
openSNPrs368282893
23andMers368282893
23andMe allrs368282893
SNP Nexus

SNPshotrs368282893
SNPdbers368282893
MSV3drs368282893
GWAS Ctlgrs368282893
Max Magnitude0
ClinVar
Risk rs368282893(T;T)
Alt rs368282893(T;T)
Reference rs368282893(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TTN
CLNDBN not specified not provided
Reversed 0
HGVS NC_000002.11:g.179647024C>T
CLNSRC
CLNACC RCV000040208.2, RCV000171326.1,