rs137852577

Orientation

plus

Stabilized

plus

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

Make rs137852577(C;T)

Make rs137852577(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67722898

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852577
dbSNP (classic)	rs137852577
ClinGen	rs137852577
ebi	rs137852577
HLI	rs137852577
Exac	rs137852577
Gnomad	rs137852577
Varsome	rs137852577
LitVar	rs137852577
Map	rs137852577
PheGenI	rs137852577
Biobank	rs137852577
1000 genomes	rs137852577
hgdp	rs137852577
ensembl	rs137852577
geneview	rs137852577
scholar	rs137852577
google	rs137852577
pharmgkb	rs137852577
gwascentral	rs137852577
openSNP	rs137852577
23andMe	rs137852577
SNPshot	rs137852577
SNPdbe	rs137852577
MSV3d	rs137852577
GWAS Ctlg	rs137852577

Max Magnitude

0

OMIM	313700
Desc
Variant	0026
Related	also

ClinVar
Risk	rs137852577(T;T)
Alt	rs137852577(T;T)
Reference	Rs137852577(C;C)
Significance	Pathogenic
Disease	Reifenstein syndrome Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66942740C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010504.2, RCV000010529.3,