rs137852581

Orientation

plus

Stabilized

plus

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

Make rs137852581(C;T)

Make rs137852581(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67723701

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852581
dbSNP (classic)	rs137852581
ClinGen	rs137852581
ebi	rs137852581
HLI	rs137852581
Exac	rs137852581
Gnomad	rs137852581
Varsome	rs137852581
LitVar	rs137852581
Map	rs137852581
PheGenI	rs137852581
Biobank	rs137852581
1000 genomes	rs137852581
hgdp	rs137852581
ensembl	rs137852581
geneview	rs137852581
scholar	rs137852581
google	rs137852581
pharmgkb	rs137852581
gwascentral	rs137852581
openSNP	rs137852581
23andMe	rs137852581
SNPshot	rs137852581
SNPdbe	rs137852581
MSV3d	rs137852581
GWAS Ctlg	rs137852581

Max Magnitude

0

OMIM	313700
Desc
Variant	0030
Related	also

ClinVar
Risk	rs137852581(T;T)
Alt	rs137852581(T;T)
Reference	Rs137852581(C;C)
Significance	Pathogenic
Disease	Malignant tumor of prostate
Variation	info
Gene	AR
CLNDBN	Malignant tumor of prostate
Reversed	0
HGVS	NC_000023.10:g.66943543C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010508.4,