rs1057523747

Orientation

plus

Stabilized

plus

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

Make rs1057523747(G;T)

Make rs1057523747(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

67717562

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs1057523747
dbSNP (classic)	rs1057523747
ClinGen	rs1057523747
ebi	rs1057523747
HLI	rs1057523747
Exac	rs1057523747
Gnomad	rs1057523747
Varsome	rs1057523747
LitVar	rs1057523747
Map	rs1057523747
PheGenI	rs1057523747
Biobank	rs1057523747
1000 genomes	rs1057523747
hgdp	rs1057523747
ensembl	rs1057523747
geneview	rs1057523747
scholar	rs1057523747
google	rs1057523747
pharmgkb	rs1057523747
gwascentral	rs1057523747
openSNP	rs1057523747
23andMe	rs1057523747
SNPshot	rs1057523747
SNPdbe	rs1057523747
MSV3d	rs1057523747
GWAS Ctlg	rs1057523747

Max Magnitude

0

ClinVar
Risk	rs1057523747(T;T)
Alt	rs1057523747(T;T)
Reference	Rs1057523747(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	AR
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.66937404G>T
CLNSRC
CLNACC	RCV000432265.1,