rs869320731

Orientation

plus

Stabilized

plus

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

Make rs869320731(-;-)

Make rs869320731(-;GC)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

67545326

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs869320731
dbSNP (classic)	rs869320731
ClinGen	rs869320731
ebi	rs869320731
HLI	rs869320731
Exac	rs869320731
Gnomad	rs869320731
Varsome	rs869320731
LitVar	rs869320731
Map	rs869320731
PheGenI	rs869320731
Biobank	rs869320731
1000 genomes	rs869320731
hgdp	rs869320731
ensembl	rs869320731
geneview	rs869320731
scholar	rs869320731
google	rs869320731
pharmgkb	rs869320731
gwascentral	rs869320731
openSNP	rs869320731
23andMe	rs869320731
SNPshot	rs869320731
SNPdbe	rs869320731
MSV3d	rs869320731
GWAS Ctlg	rs869320731

Max Magnitude

0

ClinVar
Risk	rs869320731(-;-)
Alt	rs869320731(-;-)
Reference	Rs869320731(GC;GC)
Significance	Pathogenic
Disease	Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66765168_66765169delGC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010489.3,