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rs869320731

From SNPedia

Orientationplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs869320731(-;-)
Make rs869320731(-;GC)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position67545326
GeneAR
is asnp
is mentioned by
dbSNPrs869320731
ebirs869320731
HLIrs869320731
Exacrs869320731
Varsomers869320731
Maprs869320731
PheGenIrs869320731
hapmaprs869320731
1000 genomesrs869320731
hgdprs869320731
ensemblrs869320731
gopubmedrs869320731
geneviewrs869320731
scholarrs869320731
googlers869320731
pharmgkbrs869320731
gwascentralrs869320731
openSNPrs869320731
23andMers869320731
23andMe allrs869320731
SNP Nexus

SNPshotrs869320731
SNPdbers869320731
MSV3drs869320731
GWAS Ctlgrs869320731
Max Magnitude0
ClinVar
Risk rs869320731(;)
Alt rs869320731(;)
Reference rs869320731(GC;GC)
Significance Pathogenic
Disease Androgen resistance syndrome
Variation info
Gene AR
CLNDBN Androgen resistance syndrome
Reversed 0
HGVS NC_000023.10:g.66765168_66765169delGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000010489.2,