rs1057521121

Orientation

plus

Stabilized

plus

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

Make rs1057521121(C;C)

Make rs1057521121(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

67643359

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs1057521121
dbSNP (classic)	rs1057521121
ClinGen	rs1057521121
ebi	rs1057521121
HLI	rs1057521121
Exac	rs1057521121
Gnomad	rs1057521121
Varsome	rs1057521121
LitVar	rs1057521121
Map	rs1057521121
PheGenI	rs1057521121
Biobank	rs1057521121
1000 genomes	rs1057521121
hgdp	rs1057521121
ensembl	rs1057521121
geneview	rs1057521121
scholar	rs1057521121
google	rs1057521121
pharmgkb	rs1057521121
gwascentral	rs1057521121
openSNP	rs1057521121
23andMe	rs1057521121
SNPshot	rs1057521121
SNPdbe	rs1057521121
MSV3d	rs1057521121
GWAS Ctlg	rs1057521121

Max Magnitude

0

ClinVar
Risk	rs1057521121(C;C)
Alt	rs1057521121(C;C)
Reference	Rs1057521121(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	AR
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.66863201G>C
CLNSRC
CLNACC	RCV000431825.1,