rs137852593

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs137852593(G;T)

Make rs137852593(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67717484

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852593
dbSNP (classic)	rs137852593
ClinGen	rs137852593
ebi	rs137852593
HLI	rs137852593
Exac	rs137852593
Gnomad	rs137852593
Varsome	rs137852593
LitVar	rs137852593
Map	rs137852593
PheGenI	rs137852593
Biobank	rs137852593
1000 genomes	rs137852593
hgdp	rs137852593
ensembl	rs137852593
geneview	rs137852593
scholar	rs137852593
google	rs137852593
pharmgkb	rs137852593
gwascentral	rs137852593
openSNP	rs137852593
23andMe	rs137852593
SNPshot	rs137852593
SNPdbe	rs137852593
MSV3d	rs137852593
GWAS Ctlg	rs137852593

GMAF

0.0

Max Magnitude

0

OMIM	313700
Desc
Variant	0047
Related	also

ClinVar
Risk	rs137852593(A;A) rs137852593(C;C) rs137852593(T;T)
Alt	rs137852593(A;A) rs137852593(C;C) rs137852593(T;T)
Reference	Rs137852593(G;G)
Significance	Pathogenic
Disease	Prostate cancer susceptibility
Variation	info
Gene	AR
CLNDBN	Prostate cancer susceptibility
Reversed	0
HGVS	NC_000023.10:g.66937326G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010523.4,