rs137852599

Orientation

plus

Stabilized

plus

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

Make rs137852599(A;C)

Make rs137852599(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67711585

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852599
dbSNP (classic)	rs137852599
ClinGen	rs137852599
ebi	rs137852599
HLI	rs137852599
Exac	rs137852599
Gnomad	rs137852599
Varsome	rs137852599
LitVar	rs137852599
Map	rs137852599
PheGenI	rs137852599
Biobank	rs137852599
1000 genomes	rs137852599
hgdp	rs137852599
ensembl	rs137852599
geneview	rs137852599
scholar	rs137852599
google	rs137852599
pharmgkb	rs137852599
gwascentral	rs137852599
openSNP	rs137852599
23andMe	rs137852599
SNPshot	rs137852599
SNPdbe	rs137852599
MSV3d	rs137852599
GWAS Ctlg	rs137852599

Max Magnitude

0

OMIM	313700
Desc
Variant	0055
Related	also

ClinVar
Risk	rs137852599(C;C)
Alt	rs137852599(C;C)
Reference	Rs137852599(A;A)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66931427A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010530.4,