rs137852566

Orientation

plus

Stabilized

plus

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

Make rs137852566(A;T)

Make rs137852566(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67686012

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852566
dbSNP (classic)	rs137852566
ClinGen	rs137852566
ebi	rs137852566
HLI	rs137852566
Exac	rs137852566
Gnomad	rs137852566
Varsome	rs137852566
LitVar	rs137852566
Map	rs137852566
PheGenI	rs137852566
Biobank	rs137852566
1000 genomes	rs137852566
hgdp	rs137852566
ensembl	rs137852566
geneview	rs137852566
scholar	rs137852566
google	rs137852566
pharmgkb	rs137852566
gwascentral	rs137852566
openSNP	rs137852566
23andMe	rs137852566
SNPshot	rs137852566
SNPdbe	rs137852566
MSV3d	rs137852566
GWAS Ctlg	rs137852566

Max Magnitude

0

OMIM	313700
Desc
Variant	0007
Related	also

ClinVar
Risk	rs137852566(T;T)
Alt	rs137852566(T;T)
Reference	Rs137852566(A;A)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66905854A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010482.3,