rs137852569

Orientation

plus

Stabilized

plus

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

Make rs137852569(A;A)

Make rs137852569(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67686030

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852569
dbSNP (classic)	rs137852569
ClinGen	rs137852569
ebi	rs137852569
HLI	rs137852569
Exac	rs137852569
Gnomad	rs137852569
Varsome	rs137852569
LitVar	rs137852569
Map	rs137852569
PheGenI	rs137852569
Biobank	rs137852569
1000 genomes	rs137852569
hgdp	rs137852569
ensembl	rs137852569
geneview	rs137852569
scholar	rs137852569
google	rs137852569
pharmgkb	rs137852569
gwascentral	rs137852569
openSNP	rs137852569
23andMe	rs137852569
SNPshot	rs137852569
SNPdbe	rs137852569
MSV3d	rs137852569
GWAS Ctlg	rs137852569

Max Magnitude

0

OMIM	313700
Desc
Variant	0011
Related	also

ClinVar
Risk	rs137852569(A;A)
Alt	rs137852569(A;A)
Reference	Rs137852569(G;G)
Significance	Pathogenic
Disease	Reifenstein syndrome
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome
Reversed	0
HGVS	NC_000023.10:g.66905872G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010487.2,