rs1800053

Orientation

plus

Stabilized

plus

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

Make rs1800053(A;A)

Make rs1800053(A;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67711453

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs1800053
dbSNP (classic)	rs1800053
ClinGen	rs1800053
ebi	rs1800053
HLI	rs1800053
Exac	rs1800053
Gnomad	rs1800053
Varsome	rs1800053
LitVar	rs1800053
Map	rs1800053
PheGenI	rs1800053
Biobank	rs1800053
1000 genomes	rs1800053
hgdp	rs1800053
ensembl	rs1800053
geneview	rs1800053
scholar	rs1800053
google	rs1800053
pharmgkb	rs1800053
gwascentral	rs1800053
openSNP	rs1800053
23andMe	rs1800053
SNPshot	rs1800053
SNPdbe	rs1800053
MSV3d	rs1800053
GWAS Ctlg	rs1800053

Max Magnitude

0

OMIM	313700
Desc
Variant	0060
Related	also

ClinVar
Risk	rs1800053(A;A)
Alt	rs1800053(A;A)
Reference	Rs1800053(C;C)
Significance	Pathogenic
Disease	Reifenstein syndrome
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome
Reversed	0
HGVS	NC_000023.10:g.66931295C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010536.2,