Have questions? Visit https://www.reddit.com/r/SNPedia

rs534237033

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs534237033(C;T)
Make rs534237033(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position95512589
GeneTTC37
is asnp
is mentioned by
dbSNPrs534237033
ebirs534237033
HLIrs534237033
Exacrs534237033
Varsomers534237033
Maprs534237033
PheGenIrs534237033
hapmaprs534237033
1000 genomesrs534237033
hgdprs534237033
ensemblrs534237033
gopubmedrs534237033
geneviewrs534237033
scholarrs534237033
googlers534237033
pharmgkbrs534237033
gwascentralrs534237033
openSNPrs534237033
23andMers534237033
23andMe allrs534237033
SNP Nexus

SNPshotrs534237033
SNPdbers534237033
MSV3drs534237033
GWAS Ctlgrs534237033
Max Magnitude0
ClinVar
Risk rs534237033(T;T)
Alt rs534237033(T;T)
Reference rs534237033(C;C)
Significance Pathogenic
Disease Trichohepatoenteric syndrome
Variation info
Gene TTC37
CLNDBN Trichohepatoenteric syndrome
Reversed 0
HGVS NC_000005.9:g.94848293C>T
CLNSRC
CLNACC RCV000176881.1,