rs137852601

Orientation

plus

Stabilized

plus

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

Make rs137852601(C;G)

Make rs137852601(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67717526

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852601
dbSNP (classic)	rs137852601
ClinGen	rs137852601
ebi	rs137852601
HLI	rs137852601
Exac	rs137852601
Gnomad	rs137852601
Varsome	rs137852601
LitVar	rs137852601
Map	rs137852601
PheGenI	rs137852601
Biobank	rs137852601
1000 genomes	rs137852601
hgdp	rs137852601
ensembl	rs137852601
geneview	rs137852601
scholar	rs137852601
google	rs137852601
pharmgkb	rs137852601
gwascentral	rs137852601
openSNP	rs137852601
23andMe	rs137852601
SNPshot	rs137852601
SNPdbe	rs137852601
MSV3d	rs137852601
GWAS Ctlg	rs137852601

Max Magnitude

0

OMIM	313700
Desc
Variant	0059
Related	also

ClinVar
Risk	rs137852601(G;G)
Alt	rs137852601(G;G)
Reference	Rs137852601(C;C)
Significance	Pathogenic
Disease	Reifenstein syndrome
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome
Reversed	0
HGVS	NC_000023.10:g.66937368C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010535.5,