rs137852564

Orientation

plus

Stabilized

plus

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

Make rs137852564(A;A)

Make rs137852564(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67722976

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852564
dbSNP (classic)	rs137852564
ClinGen	rs137852564
ebi	rs137852564
HLI	rs137852564
Exac	rs137852564
Gnomad	rs137852564
Varsome	rs137852564
LitVar	rs137852564
Map	rs137852564
PheGenI	rs137852564
Biobank	rs137852564
1000 genomes	rs137852564
hgdp	rs137852564
ensembl	rs137852564
geneview	rs137852564
scholar	rs137852564
google	rs137852564
pharmgkb	rs137852564
gwascentral	rs137852564
openSNP	rs137852564
23andMe	rs137852564
SNPshot	rs137852564
SNPdbe	rs137852564
MSV3d	rs137852564
GWAS Ctlg	rs137852564

Max Magnitude

0

OMIM	313700
Desc
Variant	0005
Related	also

OMIM	313700
Desc
Variant	0018
Related	also

ClinVar
Risk	rs137852564(A;A) rs137852564(T;T)
Alt	rs137852564(A;A) rs137852564(T;T)
Reference	Rs137852564(G;G)
Significance	Pathogenic
Disease	Androgen resistance syndrome Reifenstein syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome Reifenstein syndrome
Reversed	0
HGVS	NC_000023.10:g.66942818G>A; NC_000023.10:g.66942818G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010480.6, RCV000010496.2,