rs137852589

Orientation

plus

Stabilized

plus

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

Make rs137852589(G;T)

Make rs137852589(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67721857

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852589
dbSNP (classic)	rs137852589
ClinGen	rs137852589
ebi	rs137852589
HLI	rs137852589
Exac	rs137852589
Gnomad	rs137852589
Varsome	rs137852589
LitVar	rs137852589
Map	rs137852589
PheGenI	rs137852589
Biobank	rs137852589
1000 genomes	rs137852589
hgdp	rs137852589
ensembl	rs137852589
geneview	rs137852589
scholar	rs137852589
google	rs137852589
pharmgkb	rs137852589
gwascentral	rs137852589
openSNP	rs137852589
23andMe	rs137852589
SNPshot	rs137852589
SNPdbe	rs137852589
MSV3d	rs137852589
GWAS Ctlg	rs137852589

Max Magnitude

0

OMIM	313700
Desc
Variant	0039
Related	also

ClinVar
Risk	rs137852589(T;T)
Alt	rs137852589(T;T)
Reference	Rs137852589(G;G)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66941699G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010516.2,