rs104894742

Orientation

plus

Stabilized

plus

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

Make rs104894742(A;A)

Make rs104894742(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67545150

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs104894742
dbSNP (classic)	rs104894742
ClinGen	rs104894742
ebi	rs104894742
HLI	rs104894742
Exac	rs104894742
Gnomad	rs104894742
Varsome	rs104894742
LitVar	rs104894742
Map	rs104894742
PheGenI	rs104894742
Biobank	rs104894742
1000 genomes	rs104894742
hgdp	rs104894742
ensembl	rs104894742
geneview	rs104894742
scholar	rs104894742
google	rs104894742
pharmgkb	rs104894742
gwascentral	rs104894742
openSNP	rs104894742
23andMe	rs104894742
SNPshot	rs104894742
SNPdbe	rs104894742
MSV3d	rs104894742
GWAS Ctlg	rs104894742

Max Magnitude

0

OMIM	313700
Desc
Variant	0038
Related	also

ClinVar
Risk	rs104894742(A;A)
Alt	rs104894742(A;A)
Reference	Rs104894742(G;G)
Significance	Pathogenic
Disease	Reifenstein syndrome
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome
Reversed	0
HGVS	NC_000023.10:g.66764992G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010515.3,