rs137852598

Orientation

plus

Stabilized

plus

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

Make rs137852598(C;G)

Make rs137852598(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67722948

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852598
dbSNP (classic)	rs137852598
ClinGen	rs137852598
ebi	rs137852598
HLI	rs137852598
Exac	rs137852598
Gnomad	rs137852598
Varsome	rs137852598
LitVar	rs137852598
Map	rs137852598
PheGenI	rs137852598
Biobank	rs137852598
1000 genomes	rs137852598
hgdp	rs137852598
ensembl	rs137852598
geneview	rs137852598
scholar	rs137852598
google	rs137852598
pharmgkb	rs137852598
gwascentral	rs137852598
openSNP	rs137852598
23andMe	rs137852598
SNPshot	rs137852598
SNPdbe	rs137852598
MSV3d	rs137852598
GWAS Ctlg	rs137852598

Max Magnitude

0

OMIM	313700
Desc
Variant	0053
Related	also

ClinVar
Risk	rs137852598(G;G) rs137852598(T;T)
Alt	rs137852598(G;G) rs137852598(T;T)
Reference	Rs137852598(C;C)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66942790C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010490.4,