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rs137852600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852600(G;T)
Make rs137852600(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67717535
GeneAR
is asnp
is mentioned by
dbSNPrs137852600
ebirs137852600
HLIrs137852600
Exacrs137852600
Varsomers137852600
Maprs137852600
PheGenIrs137852600
hapmaprs137852600
1000 genomesrs137852600
hgdprs137852600
ensemblrs137852600
gopubmedrs137852600
geneviewrs137852600
scholarrs137852600
googlers137852600
pharmgkbrs137852600
gwascentralrs137852600
openSNPrs137852600
23andMers137852600
23andMe allrs137852600
SNP Nexus

SNPshotrs137852600
SNPdbers137852600
MSV3drs137852600
GWAS Ctlgrs137852600
Max Magnitude0
OMIM313700
Desc
Variant0056
Relatedalso
OMIM313700
Desc
Variant0057
Relatedalso
ClinVar
Risk rs137852600(A,T;A,T)
Alt rs137852600(A,T;A,T)
Reference rs137852600(G;G)
Significance Pathogenic
Disease Androgen resistance syndrome Reifenstein syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome Reifenstein syndrome
Reversed 0
HGVS NC_000023.10:g.66937377G>A; NC_000023.10:g.66937377G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010533.3, RCV000010531.2, RCV000010532.2,