rs201934623

Orientation

plus

Stabilized

plus

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

Make rs201934623(C;T)

Make rs201934623(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

67546320

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs201934623
dbSNP (classic)	rs201934623
ClinGen	rs201934623
ebi	rs201934623
HLI	rs201934623
Exac	rs201934623
Gnomad	rs201934623
Varsome	rs201934623
LitVar	rs201934623
Map	rs201934623
PheGenI	rs201934623
Biobank	rs201934623
1000 genomes	rs201934623
hgdp	rs201934623
ensembl	rs201934623
geneview	rs201934623
scholar	rs201934623
google	rs201934623
pharmgkb	rs201934623
gwascentral	rs201934623
openSNP	rs201934623
23andMe	rs201934623
SNPshot	rs201934623
SNPdbe	rs201934623
MSV3d	rs201934623
GWAS Ctlg	rs201934623

Max Magnitude

0

ClinVar
Risk	rs201934623(T;T)
Alt	rs201934623(T;T)
Reference	Rs201934623(C;C)
Significance	Pathogenic
Disease	Reifenstein syndrome
Variation	info
Gene	AR
CLNDBN	Reifenstein syndrome
Reversed	0
HGVS	NC_000023.10:g.66766162C>T
CLNSRC
CLNACC	RCV000196772.1,