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rs137852566

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852566(A;T)
Make rs137852566(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67686012
GeneAR
is asnp
is mentioned by
dbSNPrs137852566
ebirs137852566
HLIrs137852566
Exacrs137852566
Varsomers137852566
Maprs137852566
PheGenIrs137852566
hapmaprs137852566
1000 genomesrs137852566
hgdprs137852566
ensemblrs137852566
gopubmedrs137852566
geneviewrs137852566
scholarrs137852566
googlers137852566
pharmgkbrs137852566
gwascentralrs137852566
openSNPrs137852566
23andMers137852566
23andMe allrs137852566
SNP Nexus

SNPshotrs137852566
SNPdbers137852566
MSV3drs137852566
GWAS Ctlgrs137852566
Max Magnitude0
OMIM313700
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137852566(T;T)
Alt rs137852566(T;T)
Reference rs137852566(A;A)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66905854A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010482.3,