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rs104894608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894608(C;T)
Make rs104894608(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position56594891
GeneNOG
is asnp
is mentioned by
dbSNPrs104894608
ebirs104894608
HLIrs104894608
Exacrs104894608
Varsomers104894608
Maprs104894608
PheGenIrs104894608
hapmaprs104894608
1000 genomesrs104894608
hgdprs104894608
ensemblrs104894608
gopubmedrs104894608
geneviewrs104894608
scholarrs104894608
googlers104894608
pharmgkbrs104894608
gwascentralrs104894608
openSNPrs104894608
23andMers104894608
23andMe allrs104894608
SNP Nexus

SNPshotrs104894608
SNPdbers104894608
MSV3drs104894608
GWAS Ctlgrs104894608
Max Magnitude0
OMIM602991
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894608(T;T)
Alt rs104894608(T;T)
Reference rs104894608(C;C)
Significance Pathogenic
Disease Cushing's symphalangism
Variation info
Gene NOG
CLNDBN Cushing's symphalangism
Reversed 0
HGVS NC_000017.10:g.54672252C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007082.3,