rs137852565

Orientation

plus

Stabilized

plus

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

Make rs137852565(A;A)

Make rs137852565(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67721905

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852565
dbSNP (classic)	rs137852565
ClinGen	rs137852565
ebi	rs137852565
HLI	rs137852565
Exac	rs137852565
Gnomad	rs137852565
Varsome	rs137852565
LitVar	rs137852565
Map	rs137852565
PheGenI	rs137852565
Biobank	rs137852565
1000 genomes	rs137852565
hgdp	rs137852565
ensembl	rs137852565
geneview	rs137852565
scholar	rs137852565
google	rs137852565
pharmgkb	rs137852565
gwascentral	rs137852565
openSNP	rs137852565
23andMe	rs137852565
SNPshot	rs137852565
SNPdbe	rs137852565
MSV3d	rs137852565
GWAS Ctlg	rs137852565

Max Magnitude

0

OMIM	313700
Desc
Variant	0006
Related	also

ClinVar
Risk	rs137852565(A;A) rs137852565(C;C)
Alt	rs137852565(A;A) rs137852565(C;C)
Reference	Rs137852565(G;G)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66941747G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010481.2,