rs137852578

Orientation

plus

Stabilized

plus

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

Make rs137852578(A;G)

Make rs137852578(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67723710

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852578
dbSNP (classic)	rs137852578
ClinGen	rs137852578
ebi	rs137852578
HLI	rs137852578
Exac	rs137852578
Gnomad	rs137852578
Varsome	rs137852578
LitVar	rs137852578
Map	rs137852578
PheGenI	rs137852578
Biobank	rs137852578
1000 genomes	rs137852578
hgdp	rs137852578
ensembl	rs137852578
geneview	rs137852578
scholar	rs137852578
google	rs137852578
pharmgkb	rs137852578
gwascentral	rs137852578
openSNP	rs137852578
23andMe	rs137852578
SNPshot	rs137852578
SNPdbe	rs137852578
MSV3d	rs137852578
GWAS Ctlg	rs137852578

Max Magnitude

0

OMIM	313700
Desc
Variant	0027
Related	also

ClinVar
Risk	rs137852578(G;G)
Alt	rs137852578(G;G)
Reference	Rs137852578(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.66943552A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010505.4,