rs1057518177

Orientation

plus

Stabilized

plus

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

Make rs1057518177(-;-)

Make rs1057518177(-;CCATTGAGCCAGGTGTAG)

Make rs1057518177(CCATTGAGCCAGGTGTAG;CCATTGAGCCAGGTGTAG)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

67711555

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs1057518177
dbSNP (classic)	rs1057518177
ClinGen	rs1057518177
ebi	rs1057518177
HLI	rs1057518177
Exac	rs1057518177
Gnomad	rs1057518177
Varsome	rs1057518177
LitVar	rs1057518177
Map	rs1057518177
PheGenI	rs1057518177
Biobank	rs1057518177
1000 genomes	rs1057518177
hgdp	rs1057518177
ensembl	rs1057518177
geneview	rs1057518177
scholar	rs1057518177
google	rs1057518177
pharmgkb	rs1057518177
gwascentral	rs1057518177
openSNP	rs1057518177
23andMe	rs1057518177
SNPshot	rs1057518177
SNPdbe	rs1057518177
MSV3d	rs1057518177
GWAS Ctlg	rs1057518177

Max Magnitude

0

ClinVar
Risk	rs1057518177(-;-)
Alt	rs1057518177(-;-)
Reference	Rs1057518177(AGCCATTGAGCCAGGTGT;AGCCATTGAGCCAGGTGT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	AR
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.66931397_66931414del18
CLNSRC
CLNACC	RCV000414028.1,