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rs387907147

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907147(C;T)
Make rs387907147(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position95540794
GeneTTC37
is asnp
is mentioned by
dbSNPrs387907147
ebirs387907147
HLIrs387907147
Exacrs387907147
Varsomers387907147
Maprs387907147
PheGenIrs387907147
hapmaprs387907147
1000 genomesrs387907147
hgdprs387907147
ensemblrs387907147
gopubmedrs387907147
geneviewrs387907147
scholarrs387907147
googlers387907147
pharmgkbrs387907147
gwascentralrs387907147
openSNPrs387907147
23andMers387907147
23andMe allrs387907147
SNP Nexus

SNPshotrs387907147
SNPdbers387907147
MSV3drs387907147
GWAS Ctlgrs387907147
Max Magnitude0
ClinVar
Risk rs387907147(T;T)
Alt rs387907147(T;T)
Reference rs387907147(C;C)
Significance Pathogenic
Disease Trichohepatoenteric syndrome
Variation info
Gene TTC37
CLNDBN Trichohepatoenteric syndrome
Reversed 1
HGVS NC_000005.9:g.94876498G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024232.3,