rs137852567

Orientation

plus

Stabilized

plus

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

Make rs137852567(A;G)

Make rs137852567(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67717595

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852567
dbSNP (classic)	rs137852567
ClinGen	rs137852567
ebi	rs137852567
HLI	rs137852567
Exac	rs137852567
Gnomad	rs137852567
Varsome	rs137852567
LitVar	rs137852567
Map	rs137852567
PheGenI	rs137852567
Biobank	rs137852567
1000 genomes	rs137852567
hgdp	rs137852567
ensembl	rs137852567
geneview	rs137852567
scholar	rs137852567
google	rs137852567
pharmgkb	rs137852567
gwascentral	rs137852567
openSNP	rs137852567
23andMe	rs137852567
SNPshot	rs137852567
SNPdbe	rs137852567
MSV3d	rs137852567
GWAS Ctlg	rs137852567

Max Magnitude

0

OMIM	313700
Desc
Variant	0008
Related	also

ClinVar
Risk	rs137852567(G;G)
Alt	rs137852567(G;G)
Reference	Rs137852567(A;A)
Significance	Pathogenic
Disease	Reifenstein syndrome
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome
Reversed	0
HGVS	NC_000023.10:g.66937437A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010484.2,