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rs759327087

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs759327087(-;-)
Make rs759327087(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position67545325
GeneAR
is asnp
is mentioned by
dbSNPrs759327087
ebirs759327087
HLIrs759327087
Exacrs759327087
Varsomers759327087
Maprs759327087
PheGenIrs759327087
hapmaprs759327087
1000 genomesrs759327087
hgdprs759327087
ensemblrs759327087
gopubmedrs759327087
geneviewrs759327087
scholarrs759327087
googlers759327087
pharmgkbrs759327087
gwascentralrs759327087
openSNPrs759327087
23andMers759327087
23andMe allrs759327087
SNP Nexus

SNPshotrs759327087
SNPdbers759327087
MSV3drs759327087
GWAS Ctlgrs759327087
Max Magnitude0
ClinVar
Risk rs759327087(AA,AGCA;AA,AGCA)
Alt rs759327087(AA,AGCA;AA,AGCA)
Reference rs759327087(A;A)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66765167dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000010522.2,