rs9332971

Orientation

plus

Stabilized

plus

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

Make rs9332971(A;A)

Make rs9332971(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67722944

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs9332971
dbSNP (classic)	rs9332971
ClinGen	rs9332971
ebi	rs9332971
HLI	rs9332971
Exac	rs9332971
Gnomad	rs9332971
Varsome	rs9332971
LitVar	rs9332971
Map	rs9332971
PheGenI	rs9332971
Biobank	rs9332971
1000 genomes	rs9332971
hgdp	rs9332971
ensembl	rs9332971
geneview	rs9332971
scholar	rs9332971
google	rs9332971
pharmgkb	rs9332971
gwascentral	rs9332971
openSNP	rs9332971
23andMe	rs9332971
SNPshot	rs9332971
SNPdbe	rs9332971
MSV3d	rs9332971
GWAS Ctlg	rs9332971

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

OMIM	313700
Desc
Variant	0019
Related	also

ClinVar
Risk	rs9332971(A;A) rs9332971(T;T)
Alt	rs9332971(A;A) rs9332971(T;T)
Reference	Rs9332971(G;G)
Significance	Pathogenic
Disease	Reifenstein syndrome not provided
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome not provided
Reversed	0
HGVS	NC_000023.10:g.66942786G>A; NC_000023.10:g.66942786G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010497.4, RCV000349225.1,