rs137852573

Orientation

plus

Stabilized

plus

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

Make rs137852573(A;A)

Make rs137852573(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67686064

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852573
dbSNP (classic)	rs137852573
ClinGen	rs137852573
ebi	rs137852573
HLI	rs137852573
Exac	rs137852573
Gnomad	rs137852573
Varsome	rs137852573
LitVar	rs137852573
Map	rs137852573
PheGenI	rs137852573
Biobank	rs137852573
1000 genomes	rs137852573
hgdp	rs137852573
ensembl	rs137852573
geneview	rs137852573
scholar	rs137852573
google	rs137852573
pharmgkb	rs137852573
gwascentral	rs137852573
openSNP	rs137852573
23andMe	rs137852573
SNPshot	rs137852573
SNPdbe	rs137852573
MSV3d	rs137852573
GWAS Ctlg	rs137852573

Max Magnitude

0

OMIM	313700
Desc
Variant	0016
Related	also

ClinVar
Risk	rs137852573(A;A)
Alt	rs137852573(A;A)
Reference	Rs137852573(G;G)
Significance	Pathogenic
Disease	Reifenstein syndrome not provided
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome not provided
Reversed	0
HGVS	NC_000023.10:g.66905906G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010494.3, RCV000382955.1,