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rs369108107

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369108107(C;T)
Make rs369108107(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178712153
GeneTTN
is asnp
is mentioned by
dbSNPrs369108107
ebirs369108107
HLIrs369108107
Exacrs369108107
Varsomers369108107
Maprs369108107
PheGenIrs369108107
hapmaprs369108107
1000 genomesrs369108107
hgdprs369108107
ensemblrs369108107
gopubmedrs369108107
geneviewrs369108107
scholarrs369108107
googlers369108107
pharmgkbrs369108107
gwascentralrs369108107
openSNPrs369108107
23andMers369108107
23andMe allrs369108107
SNP Nexus

SNPshotrs369108107
SNPdbers369108107
MSV3drs369108107
GWAS Ctlgrs369108107
Max Magnitude0
ClinVar
Risk rs369108107(T;T)
Alt rs369108107(T;T)
Reference rs369108107(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179576880C>T
CLNSRC
CLNACC RCV000171322.1,