rs1057521122

Orientation

plus

Stabilized

plus

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

Make rs1057521122(A;G)

Make rs1057521122(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

67722881

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs1057521122
dbSNP (classic)	rs1057521122
ClinGen	rs1057521122
ebi	rs1057521122
HLI	rs1057521122
Exac	rs1057521122
Gnomad	rs1057521122
Varsome	rs1057521122
LitVar	rs1057521122
Map	rs1057521122
PheGenI	rs1057521122
Biobank	rs1057521122
1000 genomes	rs1057521122
hgdp	rs1057521122
ensembl	rs1057521122
geneview	rs1057521122
scholar	rs1057521122
google	rs1057521122
pharmgkb	rs1057521122
gwascentral	rs1057521122
openSNP	rs1057521122
23andMe	rs1057521122
SNPshot	rs1057521122
SNPdbe	rs1057521122
MSV3d	rs1057521122
GWAS Ctlg	rs1057521122

Max Magnitude

0

ClinVar
Risk	rs1057521122(G;G)
Alt	rs1057521122(G;G)
Reference	Rs1057521122(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	AR
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.66942723A>G
CLNSRC
CLNACC	RCV000441243.1,