rs137852562

Orientation

plus

Stabilized

plus

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

Make rs137852562(C;T)

Make rs137852562(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67721837

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852562
dbSNP (classic)	rs137852562
ClinGen	rs137852562
ebi	rs137852562
HLI	rs137852562
Exac	rs137852562
Gnomad	rs137852562
Varsome	rs137852562
LitVar	rs137852562
Map	rs137852562
PheGenI	rs137852562
Biobank	rs137852562
1000 genomes	rs137852562
hgdp	rs137852562
ensembl	rs137852562
geneview	rs137852562
scholar	rs137852562
google	rs137852562
pharmgkb	rs137852562
gwascentral	rs137852562
openSNP	rs137852562
23andMe	rs137852562
SNPshot	rs137852562
SNPdbe	rs137852562
MSV3d	rs137852562
GWAS Ctlg	rs137852562

Max Magnitude

0

OMIM	313700
Desc
Variant	0003
Related	also

ClinVar
Risk	rs137852562(T;T)
Alt	rs137852562(T;T)
Reference	Rs137852562(C;C)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66941679C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010478.3,