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rs121908948

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908948(G;G)
Make rs121908948(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position56594887
GeneNOG
is asnp
is mentioned by
dbSNPrs121908948
ebirs121908948
HLIrs121908948
Exacrs121908948
Varsomers121908948
Maprs121908948
PheGenIrs121908948
hapmaprs121908948
1000 genomesrs121908948
hgdprs121908948
ensemblrs121908948
gopubmedrs121908948
geneviewrs121908948
scholarrs121908948
googlers121908948
pharmgkbrs121908948
gwascentralrs121908948
openSNPrs121908948
23andMers121908948
23andMe allrs121908948
SNP Nexus

SNPshotrs121908948
SNPdbers121908948
MSV3drs121908948
GWAS Ctlgrs121908948
Max Magnitude0
OMIM602991
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908948(G;G)
Alt rs121908948(G;G)
Reference rs121908948(T;T)
Significance Pathogenic
Disease Cushing's symphalangism
Variation info
Gene NOG
CLNDBN Cushing's symphalangism
Reversed 0
HGVS NC_000017.10:g.54672248T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007080.3,