rs137852580

Orientation

plus

Stabilized

plus

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

Make rs137852580(C;G)

Make rs137852580(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67723711

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852580
dbSNP (classic)	rs137852580
ClinGen	rs137852580
ebi	rs137852580
HLI	rs137852580
Exac	rs137852580
Gnomad	rs137852580
Varsome	rs137852580
LitVar	rs137852580
Map	rs137852580
PheGenI	rs137852580
Biobank	rs137852580
1000 genomes	rs137852580
hgdp	rs137852580
ensembl	rs137852580
geneview	rs137852580
scholar	rs137852580
google	rs137852580
pharmgkb	rs137852580
gwascentral	rs137852580
openSNP	rs137852580
23andMe	rs137852580
SNPshot	rs137852580
SNPdbe	rs137852580
MSV3d	rs137852580
GWAS Ctlg	rs137852580

Max Magnitude

0

OMIM	313700
Desc
Variant	0029
Related	also

ClinVar
Risk	rs137852580(G;G)
Alt	rs137852580(G;G)
Reference	Rs137852580(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.66943553C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010507.3,