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rs1060499527

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499527(-;-)
Make rs1060499527(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position95523654
GeneTTC37
is asnp
is mentioned by
dbSNPrs1060499527
dbSNP (old)rs1060499527
ClinGenrs1060499527
ebirs1060499527
HLIrs1060499527
Exacrs1060499527
Gnomadrs1060499527
Varsomers1060499527
LitVarrs1060499527
Maprs1060499527
PheGenIrs1060499527
Biobankrs1060499527
1000 genomesrs1060499527
hgdprs1060499527
ensemblrs1060499527
gopubmedrs1060499527
geneviewrs1060499527
scholarrs1060499527
googlers1060499527
pharmgkbrs1060499527
gwascentralrs1060499527
openSNPrs1060499527
23andMers1060499527
23andMe allrs1060499527
SNPshotrs1060499527
SNPdbers1060499527
MSV3drs1060499527
GWAS Ctlgrs1060499527
Max Magnitude0
ClinVar
Risk rs1060499527(-;-)
Alt rs1060499527(-;-)
Reference Rs1060499527(G;G)
Significance Pathogenic
Disease Trichohepatoenteric syndrome 1
Variation info
Gene TTC37
CLNDBN Trichohepatoenteric syndrome 1
Reversed 1
HGVS NC_000005.9:g.94859358delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000024231.3,