rs753933273

Orientation

plus

Stabilized

plus

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

Make rs753933273(A;A)

Make rs753933273(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

157084773

Gene

ARID1B

is a	snp
is	mentioned by
dbSNP	rs753933273
dbSNP (classic)	rs753933273
ClinGen	rs753933273
ebi	rs753933273
HLI	rs753933273
Exac	rs753933273
Gnomad	rs753933273
Varsome	rs753933273
LitVar	rs753933273
Map	rs753933273
PheGenI	rs753933273
Biobank	rs753933273
1000 genomes	rs753933273
hgdp	rs753933273
ensembl	rs753933273
geneview	rs753933273
scholar	rs753933273
google	rs753933273
pharmgkb	rs753933273
gwascentral	rs753933273
openSNP	rs753933273
23andMe	rs753933273
SNPshot	rs753933273
SNPdbe	rs753933273
MSV3d	rs753933273
GWAS Ctlg	rs753933273

Max Magnitude

0

ClinVar
Risk	rs753933273(A;A) rs753933273(T;T)
Alt	rs753933273(A;A) rs753933273(T;T)
Reference	Rs753933273(C;C)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	ARID1B
CLNDBN	Mental retardation, autosomal dominant 12
Reversed	0
HGVS	NC_000006.11:g.157405907C>T
CLNSRC
CLNACC	RCV000195185.1,