rs137852572

Orientation

plus

Stabilized

plus

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

Make rs137852572(A;A)

Make rs137852572(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67721838

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852572
dbSNP (classic)	rs137852572
ClinGen	rs137852572
ebi	rs137852572
HLI	rs137852572
Exac	rs137852572
Gnomad	rs137852572
Varsome	rs137852572
LitVar	rs137852572
Map	rs137852572
PheGenI	rs137852572
Biobank	rs137852572
1000 genomes	rs137852572
hgdp	rs137852572
ensembl	rs137852572
geneview	rs137852572
scholar	rs137852572
google	rs137852572
pharmgkb	rs137852572
gwascentral	rs137852572
openSNP	rs137852572
23andMe	rs137852572
SNPshot	rs137852572
SNPdbe	rs137852572
MSV3d	rs137852572
GWAS Ctlg	rs137852572

Max Magnitude

0

OMIM	313700
Desc
Variant	0015
Related	also

ClinVar
Risk	rs137852572(A;A)
Alt	rs137852572(A;A)
Reference	Rs137852572(G;G)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66941680G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010493.2,