rs137852570

Orientation

plus

Stabilized

plus

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

Make rs137852570(A;G)

Make rs137852570(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67721876

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852570
dbSNP (classic)	rs137852570
ClinGen	rs137852570
ebi	rs137852570
HLI	rs137852570
Exac	rs137852570
Gnomad	rs137852570
Varsome	rs137852570
LitVar	rs137852570
Map	rs137852570
PheGenI	rs137852570
Biobank	rs137852570
1000 genomes	rs137852570
hgdp	rs137852570
ensembl	rs137852570
geneview	rs137852570
scholar	rs137852570
google	rs137852570
pharmgkb	rs137852570
gwascentral	rs137852570
openSNP	rs137852570
23andMe	rs137852570
SNPshot	rs137852570
SNPdbe	rs137852570
MSV3d	rs137852570
GWAS Ctlg	rs137852570

Max Magnitude

0

OMIM	313700
Desc
Variant	0012
Related	also

ClinVar
Risk	rs137852570(G;G)
Alt	rs137852570(G;G)
Reference	Rs137852570(A;A)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66941718A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010488.2,