rs137852600

Orientation

plus

Stabilized

plus

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

Make rs137852600(G;T)

Make rs137852600(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67717535

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852600
dbSNP (classic)	rs137852600
ClinGen	rs137852600
ebi	rs137852600
HLI	rs137852600
Exac	rs137852600
Gnomad	rs137852600
Varsome	rs137852600
LitVar	rs137852600
Map	rs137852600
PheGenI	rs137852600
Biobank	rs137852600
1000 genomes	rs137852600
hgdp	rs137852600
ensembl	rs137852600
geneview	rs137852600
scholar	rs137852600
google	rs137852600
pharmgkb	rs137852600
gwascentral	rs137852600
openSNP	rs137852600
23andMe	rs137852600
SNPshot	rs137852600
SNPdbe	rs137852600
MSV3d	rs137852600
GWAS Ctlg	rs137852600

Max Magnitude

0

OMIM	313700
Desc
Variant	0056
Related	also

OMIM	313700
Desc
Variant	0057
Related	also

ClinVar
Risk	rs137852600(A;A) rs137852600(T;T)
Alt	rs137852600(A;A) rs137852600(T;T)
Reference	Rs137852600(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.66937377G>A; NC_000023.10:g.66937377G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010533.4, RCV000010531.3, RCV000010532.3,