rs137852590

Orientation

plus

Stabilized

plus

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

Make rs137852590(G;G)

Make rs137852590(G;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67545667

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852590
dbSNP (classic)	rs137852590
ClinGen	rs137852590
ebi	rs137852590
HLI	rs137852590
Exac	rs137852590
Gnomad	rs137852590
Varsome	rs137852590
LitVar	rs137852590
Map	rs137852590
PheGenI	rs137852590
Biobank	rs137852590
1000 genomes	rs137852590
hgdp	rs137852590
ensembl	rs137852590
geneview	rs137852590
scholar	rs137852590
google	rs137852590
pharmgkb	rs137852590
gwascentral	rs137852590
openSNP	rs137852590
23andMe	rs137852590
SNPshot	rs137852590
SNPdbe	rs137852590
MSV3d	rs137852590
GWAS Ctlg	rs137852590

Max Magnitude

0

OMIM	313700
Desc
Variant	0042
Related	also

ClinVar
Risk	rs137852590(G;G)
Alt	rs137852590(G;G)
Reference	Rs137852590(T;T)
Significance	Pathogenic
Disease	Reifenstein syndrome
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome
Reversed	0
HGVS	NC_000023.10:g.66765509T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010519.6,