rs137852571

Orientation

plus

Stabilized

plus

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

Make rs137852571(A;A)

Make rs137852571(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67717495

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852571
dbSNP (classic)	rs137852571
ClinGen	rs137852571
ebi	rs137852571
HLI	rs137852571
Exac	rs137852571
Gnomad	rs137852571
Varsome	rs137852571
LitVar	rs137852571
Map	rs137852571
PheGenI	rs137852571
Biobank	rs137852571
1000 genomes	rs137852571
hgdp	rs137852571
ensembl	rs137852571
geneview	rs137852571
scholar	rs137852571
google	rs137852571
pharmgkb	rs137852571
gwascentral	rs137852571
openSNP	rs137852571
23andMe	rs137852571
SNPshot	rs137852571
SNPdbe	rs137852571
MSV3d	rs137852571
GWAS Ctlg	rs137852571

Max Magnitude

0

OMIM	313700
Desc
Variant	0013
Related	also

ClinVar
Risk	rs137852571(A;A)
Alt	rs137852571(A;A)
Reference	Rs137852571(G;G)
Significance	Pathogenic
Disease	Malignant tumor of prostate
Variation	info
Gene	AR
CLNDBN	Malignant tumor of prostate
Reversed	0
HGVS	NC_000023.10:g.66937337G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010491.4,