rs137852575

Orientation

plus

Stabilized

plus

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

Make rs137852575(C;T)

Make rs137852575(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67545324

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852575
dbSNP (classic)	rs137852575
ClinGen	rs137852575
ebi	rs137852575
HLI	rs137852575
Exac	rs137852575
Gnomad	rs137852575
Varsome	rs137852575
LitVar	rs137852575
Map	rs137852575
PheGenI	rs137852575
Biobank	rs137852575
1000 genomes	rs137852575
hgdp	rs137852575
ensembl	rs137852575
geneview	rs137852575
scholar	rs137852575
google	rs137852575
pharmgkb	rs137852575
gwascentral	rs137852575
openSNP	rs137852575
23andMe	rs137852575
SNPshot	rs137852575
SNPdbe	rs137852575
MSV3d	rs137852575
GWAS Ctlg	rs137852575

Max Magnitude

0

OMIM	313700
Desc
Variant	0021
Related	also

ClinVar
Risk	rs137852575(T;T)
Alt	rs137852575(T;T)
Reference	Rs137852575(C;C)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66765166C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010499.2,