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

rs869320732

From SNPedia

Orientationplus
Geno Mag Summary
(AGGATGC;AGGATGC) 0 common in clinvar
Make rs869320732(AGGATGC;TTCGCCCCTGA)
Make rs869320732(TTCGCCCCTGA;TTCGCCCCTGA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position67717585
GeneAR
is asnp
is mentioned by
dbSNPrs869320732
ebirs869320732
HLIrs869320732
Exacrs869320732
Varsomers869320732
Maprs869320732
PheGenIrs869320732
hapmaprs869320732
1000 genomesrs869320732
hgdprs869320732
ensemblrs869320732
gopubmedrs869320732
geneviewrs869320732
scholarrs869320732
googlers869320732
pharmgkbrs869320732
gwascentralrs869320732
openSNPrs869320732
23andMers869320732
23andMe allrs869320732
SNP Nexus

SNPshotrs869320732
SNPdbers869320732
MSV3drs869320732
GWAS Ctlgrs869320732
Max Magnitude0
ClinVar
Risk rs869320732(TTCGCCCCTGA;TTCGCCCCTGA)
Alt rs869320732(TTCGCCCCTGA;TTCGCCCCTGA)
Reference rs869320732(AGGATGC;AGGATGC)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66937427_66937433delAGGATGCinsTTCGCCCCTGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000010534.4,