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rs137852570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852570(A;G)
Make rs137852570(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position67721876
GeneAR
is asnp
is mentioned by
dbSNPrs137852570
ebirs137852570
HLIrs137852570
Exacrs137852570
Varsomers137852570
Maprs137852570
PheGenIrs137852570
hapmaprs137852570
1000 genomesrs137852570
hgdprs137852570
ensemblrs137852570
gopubmedrs137852570
geneviewrs137852570
scholarrs137852570
googlers137852570
pharmgkbrs137852570
gwascentralrs137852570
openSNPrs137852570
23andMers137852570
23andMe allrs137852570
SNP Nexus

SNPshotrs137852570
SNPdbers137852570
MSV3drs137852570
GWAS Ctlgrs137852570
Max Magnitude0
OMIM313700
Desc
Variant0012
Relatedalso
ClinVar
Risk rs137852570(G;G)
Alt rs137852570(G;G)
Reference rs137852570(A;A)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66941718A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010488.2,