rs137852596

Orientation

plus

Stabilized

plus

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

Make rs137852596(A;A)

Make rs137852596(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67643371

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852596
dbSNP (classic)	rs137852596
ClinGen	rs137852596
ebi	rs137852596
HLI	rs137852596
Exac	rs137852596
Gnomad	rs137852596
Varsome	rs137852596
LitVar	rs137852596
Map	rs137852596
PheGenI	rs137852596
Biobank	rs137852596
1000 genomes	rs137852596
hgdp	rs137852596
ensembl	rs137852596
geneview	rs137852596
scholar	rs137852596
google	rs137852596
pharmgkb	rs137852596
gwascentral	rs137852596
openSNP	rs137852596
23andMe	rs137852596
SNPshot	rs137852596
SNPdbe	rs137852596
MSV3d	rs137852596
GWAS Ctlg	rs137852596

Max Magnitude

0

OMIM	313700
Desc
Variant	0051
Related	also

ClinVar
Risk	rs137852596(A;A)
Alt	rs137852596(A;A)
Reference	Rs137852596(G;G)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66863213G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010527.3,