rs137852586

Orientation

plus

Stabilized

plus

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

Make rs137852586(G;T)

Make rs137852586(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67643378

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852586
dbSNP (classic)	rs137852586
ClinGen	rs137852586
ebi	rs137852586
HLI	rs137852586
Exac	rs137852586
Gnomad	rs137852586
Varsome	rs137852586
LitVar	rs137852586
Map	rs137852586
PheGenI	rs137852586
Biobank	rs137852586
1000 genomes	rs137852586
hgdp	rs137852586
ensembl	rs137852586
geneview	rs137852586
scholar	rs137852586
google	rs137852586
pharmgkb	rs137852586
gwascentral	rs137852586
openSNP	rs137852586
23andMe	rs137852586
SNPshot	rs137852586
SNPdbe	rs137852586
MSV3d	rs137852586
GWAS Ctlg	rs137852586

Max Magnitude

0

OMIM	313700
Desc
Variant	0035
Related	also

ClinVar
Risk	rs137852586(T;T)
Alt	rs137852586(T;T)
Reference	Rs137852586(G;G)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66863220G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010512.2,