Have questions? Visit https://www.reddit.com/r/SNPedia

rs9332971

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9332971(A;A)
Make rs9332971(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67722944
GeneAR
is asnp
is mentioned by
dbSNPrs9332971
ClinGenrs9332971
ebirs9332971
HLIrs9332971
Exacrs9332971
Varsomers9332971
Maprs9332971
PheGenIrs9332971
hapmaprs9332971
1000 genomesrs9332971
hgdprs9332971
ensemblrs9332971
gopubmedrs9332971
geneviewrs9332971
scholarrs9332971
googlers9332971
pharmgkbrs9332971
gwascentralrs9332971
openSNPrs9332971
23andMers9332971
23andMe allrs9332971
SNP Nexus

SNPshotrs9332971
SNPdbers9332971
MSV3drs9332971
GWAS Ctlgrs9332971
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM313700
Desc
Variant0019
Relatedalso


ClinVar
Risk rs9332971(A;A)
Alt rs9332971(A;A)
Reference Rs9332971(G;G)
Significance Pathogenic
Disease Reifenstein syndrome
Variation info
Gene AR
CLNDBN Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66942786G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010497.4,