rs137852587

Orientation

plus

Stabilized

plus

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

Make rs137852587(A;A)

Make rs137852587(A;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67643387

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852587
dbSNP (classic)	rs137852587
ClinGen	rs137852587
ebi	rs137852587
HLI	rs137852587
Exac	rs137852587
Gnomad	rs137852587
Varsome	rs137852587
LitVar	rs137852587
Map	rs137852587
PheGenI	rs137852587
Biobank	rs137852587
1000 genomes	rs137852587
hgdp	rs137852587
ensembl	rs137852587
geneview	rs137852587
scholar	rs137852587
google	rs137852587
pharmgkb	rs137852587
gwascentral	rs137852587
openSNP	rs137852587
23andMe	rs137852587
SNPshot	rs137852587
SNPdbe	rs137852587
MSV3d	rs137852587
GWAS Ctlg	rs137852587

Max Magnitude

0

OMIM	313700
Desc
Variant	0036
Related	also

ClinVar
Risk	rs137852587(A;A)
Alt	rs137852587(A;A)
Reference	Rs137852587(T;T)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66863229T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010513.4,