rs137852576

Orientation

plus

Stabilized

plus

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

Make rs137852576(A;A)

Make rs137852576(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

67686067

Gene

AR

is a	snp
is	mentioned by
dbSNP	rs137852576
dbSNP (classic)	rs137852576
ClinGen	rs137852576
ebi	rs137852576
HLI	rs137852576
Exac	rs137852576
Gnomad	rs137852576
Varsome	rs137852576
LitVar	rs137852576
Map	rs137852576
PheGenI	rs137852576
Biobank	rs137852576
1000 genomes	rs137852576
hgdp	rs137852576
ensembl	rs137852576
geneview	rs137852576
scholar	rs137852576
google	rs137852576
pharmgkb	rs137852576
gwascentral	rs137852576
openSNP	rs137852576
23andMe	rs137852576
SNPshot	rs137852576
SNPdbe	rs137852576
MSV3d	rs137852576
GWAS Ctlg	rs137852576

Max Magnitude

0

OMIM	313700
Desc
Variant	0024
Related	also

ClinVar
Risk	rs137852576(A;A)
Alt	rs137852576(A;A)
Reference	Rs137852576(G;G)
Significance	Pathogenic
Disease	Androgen insensitivity
Variation	info
Gene	AR
CLNDBN	Androgen insensitivity, partial, with breast cancer
Reversed	0
HGVS	NC_000023.10:g.66905909G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010502.2,