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rs9332969

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9332969(A;A)
Make rs9332969(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67722899
GeneAR
is asnp
is mentioned by
dbSNPrs9332969
ebirs9332969
HLIrs9332969
Exacrs9332969
Varsomers9332969
Maprs9332969
PheGenIrs9332969
hapmaprs9332969
1000 genomesrs9332969
hgdprs9332969
ensemblrs9332969
gopubmedrs9332969
geneviewrs9332969
scholarrs9332969
googlers9332969
pharmgkbrs9332969
gwascentralrs9332969
openSNPrs9332969
23andMers9332969
23andMe allrs9332969
SNP Nexus

SNPshotrs9332969
SNPdbers9332969
MSV3drs9332969
GWAS Ctlgrs9332969
Max Magnitude0
OMIM313700
Desc
Variant0025
Relatedalso
? (A;G) (G;G)


ClinVar
Risk rs9332969(A;A)
Alt rs9332969(A;A)
Reference rs9332969(G;G)
Significance Pathogenic
Disease Reifenstein syndrome
Variation info
Gene AR
CLNDBN Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66942741G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010503.2,