rs137852568

Orientation

plus

Stabilized

plus

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

Make rs137852568(A;T)

Make rs137852568(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67723728

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852568
dbSNP (classic)	rs137852568
ClinGen	rs137852568
ebi	rs137852568
HLI	rs137852568
Exac	rs137852568
Gnomad	rs137852568
Varsome	rs137852568
LitVar	rs137852568
Map	rs137852568
PheGenI	rs137852568
Biobank	rs137852568
1000 genomes	rs137852568
hgdp	rs137852568
ensembl	rs137852568
geneview	rs137852568
scholar	rs137852568
google	rs137852568
pharmgkb	rs137852568
gwascentral	rs137852568
openSNP	rs137852568
23andMe	rs137852568
SNPshot	rs137852568
SNPdbe	rs137852568
MSV3d	rs137852568
GWAS Ctlg	rs137852568

Max Magnitude

0

OMIM	313700
Desc
Variant	0009
Related	also

ClinVar
Risk	rs137852568(T;T)
Alt	rs137852568(T;T)
Reference	Rs137852568(A;A)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66943570A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010485.2,