rs137852592

Orientation

plus

Stabilized

plus

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

Make rs137852592(C;C)

Make rs137852592(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67721937

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852592
dbSNP (classic)	rs137852592
ClinGen	rs137852592
ebi	rs137852592
HLI	rs137852592
Exac	rs137852592
Gnomad	rs137852592
Varsome	rs137852592
LitVar	rs137852592
Map	rs137852592
PheGenI	rs137852592
Biobank	rs137852592
1000 genomes	rs137852592
hgdp	rs137852592
ensembl	rs137852592
geneview	rs137852592
scholar	rs137852592
google	rs137852592
pharmgkb	rs137852592
gwascentral	rs137852592
openSNP	rs137852592
23andMe	rs137852592
SNPshot	rs137852592
SNPdbe	rs137852592
MSV3d	rs137852592
GWAS Ctlg	rs137852592

Max Magnitude

0

OMIM	313700
Desc
Variant	0044
Related	also

ClinVar
Risk	rs137852592(C;C)
Alt	rs137852592(C;C)
Reference	Rs137852592(T;T)
Significance	Pathogenic
Disease	Reifenstein syndrome
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome
Reversed	0
HGVS	NC_000023.10:g.66941779T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010521.5,