rs137852597

Orientation

plus

Stabilized

plus

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

Make rs137852597(C;C)

Make rs137852597(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67722973

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852597
dbSNP (classic)	rs137852597
ClinGen	rs137852597
ebi	rs137852597
HLI	rs137852597
Exac	rs137852597
Gnomad	rs137852597
Varsome	rs137852597
LitVar	rs137852597
Map	rs137852597
PheGenI	rs137852597
Biobank	rs137852597
1000 genomes	rs137852597
hgdp	rs137852597
ensembl	rs137852597
geneview	rs137852597
scholar	rs137852597
google	rs137852597
pharmgkb	rs137852597
gwascentral	rs137852597
openSNP	rs137852597
23andMe	rs137852597
SNPshot	rs137852597
SNPdbe	rs137852597
MSV3d	rs137852597
GWAS Ctlg	rs137852597

Max Magnitude

0

OMIM	313700
Desc
Variant	0052
Related	also

ClinVar
Risk	rs137852597(C;C)
Alt	rs137852597(C;C)
Reference	Rs137852597(T;T)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66942815T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010528.2,