rs137852588

Orientation

plus

Stabilized

plus

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

Make rs137852588(C;T)

Make rs137852588(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67643284

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852588
dbSNP (classic)	rs137852588
ClinGen	rs137852588
ebi	rs137852588
HLI	rs137852588
Exac	rs137852588
Gnomad	rs137852588
Varsome	rs137852588
LitVar	rs137852588
Map	rs137852588
PheGenI	rs137852588
Biobank	rs137852588
1000 genomes	rs137852588
hgdp	rs137852588
ensembl	rs137852588
geneview	rs137852588
scholar	rs137852588
google	rs137852588
pharmgkb	rs137852588
gwascentral	rs137852588
openSNP	rs137852588
23andMe	rs137852588
SNPshot	rs137852588
SNPdbe	rs137852588
MSV3d	rs137852588
GWAS Ctlg	rs137852588

Max Magnitude

0

OMIM	313700
Desc
Variant	0037
Related	also

ClinVar
Risk	rs137852588(T;T)
Alt	rs137852588(T;T)
Reference	Rs137852588(C;C)
Significance	Pathogenic
Disease	Hypospadias 1
Variation	info
Gene	AR
CLNDBN	Hypospadias 1, X-linked
Reversed	0
HGVS	NC_000023.10:g.66863126C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010514.4,