rs137852595

Orientation

plus

Stabilized

plus

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

Make rs137852595(C;T)

Make rs137852595(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67711653

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852595
dbSNP (classic)	rs137852595
ClinGen	rs137852595
ebi	rs137852595
HLI	rs137852595
Exac	rs137852595
Gnomad	rs137852595
Varsome	rs137852595
LitVar	rs137852595
Map	rs137852595
PheGenI	rs137852595
Biobank	rs137852595
1000 genomes	rs137852595
hgdp	rs137852595
ensembl	rs137852595
geneview	rs137852595
scholar	rs137852595
google	rs137852595
pharmgkb	rs137852595
gwascentral	rs137852595
openSNP	rs137852595
23andMe	rs137852595
SNPshot	rs137852595
SNPdbe	rs137852595
MSV3d	rs137852595
GWAS Ctlg	rs137852595

Max Magnitude

0

OMIM	313700
Desc
Variant	0050
Related	also

ClinVar
Risk	rs137852595(A;A) rs137852595(T;T)
Alt	rs137852595(A;A) rs137852595(T;T)
Reference	Rs137852595(C;C)
Significance	Pathogenic
Disease	not provided Androgen resistance syndrome
Variation	info
Gene	AR
CLNDBN	not provided Androgen resistance syndrome
Reversed	0
HGVS	NC_000023.10:g.66931495C>A; NC_000023.10:g.66931495C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000444076.1, RCV000010526.6,