rs137852585

Orientation

plus

Stabilized

plus

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

Make rs137852585(G;G)

Make rs137852585(G;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67711639

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852585
dbSNP (classic)	rs137852585
ClinGen	rs137852585
ebi	rs137852585
HLI	rs137852585
Exac	rs137852585
Gnomad	rs137852585
Varsome	rs137852585
LitVar	rs137852585
Map	rs137852585
PheGenI	rs137852585
Biobank	rs137852585
1000 genomes	rs137852585
hgdp	rs137852585
ensembl	rs137852585
geneview	rs137852585
scholar	rs137852585
google	rs137852585
pharmgkb	rs137852585
gwascentral	rs137852585
openSNP	rs137852585
23andMe	rs137852585
SNPshot	rs137852585
SNPdbe	rs137852585
MSV3d	rs137852585
GWAS Ctlg	rs137852585

Max Magnitude

0

OMIM	313700
Desc
Variant	0034
Related	also

ClinVar
Risk	rs137852585(G;G)
Alt	rs137852585(G;G)
Reference	Rs137852585(T;T)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66931481T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010511.5,