rs137852579

Orientation

plus

Stabilized

plus

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

Make rs137852579(C;C)

Make rs137852579(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67711549

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852579
dbSNP (classic)	rs137852579
ClinGen	rs137852579
ebi	rs137852579
HLI	rs137852579
Exac	rs137852579
Gnomad	rs137852579
Varsome	rs137852579
LitVar	rs137852579
Map	rs137852579
PheGenI	rs137852579
Biobank	rs137852579
1000 genomes	rs137852579
hgdp	rs137852579
ensembl	rs137852579
geneview	rs137852579
scholar	rs137852579
google	rs137852579
pharmgkb	rs137852579
gwascentral	rs137852579
openSNP	rs137852579
23andMe	rs137852579
SNPshot	rs137852579
SNPdbe	rs137852579
MSV3d	rs137852579
GWAS Ctlg	rs137852579

Max Magnitude

0

OMIM	313700
Desc
Variant	0028
Related	also

ClinVar
Risk	rs137852579(C;C)
Alt	rs137852579(C;C)
Reference	Rs137852579(T;T)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66931391T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010506.2,