rs137852594

Orientation

plus

Stabilized

plus

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

Make rs137852594(C;T)

Make rs137852594(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67723745

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852594
dbSNP (classic)	rs137852594
ClinGen	rs137852594
ebi	rs137852594
HLI	rs137852594
Exac	rs137852594
Gnomad	rs137852594
Varsome	rs137852594
LitVar	rs137852594
Map	rs137852594
PheGenI	rs137852594
Biobank	rs137852594
1000 genomes	rs137852594
hgdp	rs137852594
ensembl	rs137852594
geneview	rs137852594
scholar	rs137852594
google	rs137852594
pharmgkb	rs137852594
gwascentral	rs137852594
openSNP	rs137852594
23andMe	rs137852594
SNPshot	rs137852594
SNPdbe	rs137852594
MSV3d	rs137852594
GWAS Ctlg	rs137852594

Max Magnitude

0

OMIM	313700
Desc
Variant	0048
Related	also

ClinVar
Risk	rs137852594(T;T)
Alt	rs137852594(T;T)
Reference	Rs137852594(C;C)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66943587C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010524.4,