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rs1060499528

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499528(C;C)
Make rs1060499528(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position95516671
GeneTTC37
is asnp
is mentioned by
dbSNPrs1060499528
dbSNP (old)rs1060499528
ClinGenrs1060499528
ebirs1060499528
HLIrs1060499528
Exacrs1060499528
Gnomadrs1060499528
Varsomers1060499528
Maprs1060499528
PheGenIrs1060499528
Biobankrs1060499528
1000 genomesrs1060499528
hgdprs1060499528
ensemblrs1060499528
gopubmedrs1060499528
geneviewrs1060499528
scholarrs1060499528
googlers1060499528
pharmgkbrs1060499528
gwascentralrs1060499528
openSNPrs1060499528
23andMers1060499528
23andMe allrs1060499528
SNPshotrs1060499528
SNPdbers1060499528
MSV3drs1060499528
GWAS Ctlgrs1060499528
Max Magnitude0
ClinVar
Risk rs1060499528(C;C)
Alt rs1060499528(C;C)
Reference Rs1060499528(G;G)
Significance Pathogenic
Disease Trichohepatoenteric syndrome 1
Variation info
Gene TTC37
CLNDBN Trichohepatoenteric syndrome 1
Reversed 1
HGVS NC_000005.9:g.94852375C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024234.4,