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rs864622007

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864622007(A;A)
Make rs864622007(A;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position67711621
GeneAR
is asnp
is mentioned by
dbSNPrs864622007
ebirs864622007
HLIrs864622007
Exacrs864622007
Varsomers864622007
Maprs864622007
PheGenIrs864622007
hapmaprs864622007
1000 genomesrs864622007
hgdprs864622007
ensemblrs864622007
gopubmedrs864622007
geneviewrs864622007
scholarrs864622007
googlers864622007
pharmgkbrs864622007
gwascentralrs864622007
openSNPrs864622007
23andMers864622007
23andMe allrs864622007
SNP Nexus

SNPshotrs864622007
SNPdbers864622007
MSV3drs864622007
GWAS Ctlgrs864622007
Max Magnitude0
ClinVar
Risk rs864622007(A;A)
Alt rs864622007(A;A)
Reference rs864622007(T;T)
Significance Probable-Pathogenic
Disease Malignant tumor of prostate
Variation info
Gene AR
CLNDBN Malignant tumor of prostate
Reversed 0
HGVS NC_000023.10:g.66931463T>A
CLNSRC
CLNACC RCV000204071.1,