rs137852582

Orientation

plus

Stabilized

plus

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

Make rs137852582(A;G)

Make rs137852582(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67723786

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852582
dbSNP (classic)	rs137852582
ClinGen	rs137852582
ebi	rs137852582
HLI	rs137852582
Exac	rs137852582
Gnomad	rs137852582
Varsome	rs137852582
LitVar	rs137852582
Map	rs137852582
PheGenI	rs137852582
Biobank	rs137852582
1000 genomes	rs137852582
hgdp	rs137852582
ensembl	rs137852582
geneview	rs137852582
scholar	rs137852582
google	rs137852582
pharmgkb	rs137852582
gwascentral	rs137852582
openSNP	rs137852582
23andMe	rs137852582
SNPshot	rs137852582
SNPdbe	rs137852582
MSV3d	rs137852582
GWAS Ctlg	rs137852582

Max Magnitude

0

OMIM	313700
Desc
Variant	0031
Related	also

ClinVar
Risk	rs137852582(G;G)
Alt	rs137852582(G;G)
Reference	Rs137852582(A;A)
Significance	Pathogenic
Disease	Malignant tumor of prostate
Variation	info
Gene	AR
CLNDBN	Malignant tumor of prostate
Reversed	0
HGVS	NC_000023.10:g.66943628A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010509.2,