rs137852563

Orientation

plus

Stabilized

plus

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

Make rs137852563(A;A)

Make rs137852563(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67711673

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852563
dbSNP (classic)	rs137852563
ClinGen	rs137852563
ebi	rs137852563
HLI	rs137852563
Exac	rs137852563
Gnomad	rs137852563
Varsome	rs137852563
LitVar	rs137852563
Map	rs137852563
PheGenI	rs137852563
Biobank	rs137852563
1000 genomes	rs137852563
hgdp	rs137852563
ensembl	rs137852563
geneview	rs137852563
scholar	rs137852563
google	rs137852563
pharmgkb	rs137852563
gwascentral	rs137852563
openSNP	rs137852563
23andMe	rs137852563
SNPshot	rs137852563
SNPdbe	rs137852563
MSV3d	rs137852563
GWAS Ctlg	rs137852563

Max Magnitude

0

OMIM	313700
Desc
Variant	0004
Related	also

ClinVar
Risk	rs137852563(A;A)
Alt	rs137852563(A;A)
Reference	Rs137852563(G;G)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66931515G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010479.2,