rs794727977

Orientation

plus

Stabilized

plus

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

Make rs794727977(C;T)

Make rs794727977(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

157148764

Gene

ARID1B

is a	snp
is	mentioned by
dbSNP	rs794727977
dbSNP (classic)	rs794727977
ClinGen	rs794727977
ebi	rs794727977
HLI	rs794727977
Exac	rs794727977
Gnomad	rs794727977
Varsome	rs794727977
LitVar	rs794727977
Map	rs794727977
PheGenI	rs794727977
Biobank	rs794727977
1000 genomes	rs794727977
hgdp	rs794727977
ensembl	rs794727977
geneview	rs794727977
scholar	rs794727977
google	rs794727977
pharmgkb	rs794727977
gwascentral	rs794727977
openSNP	rs794727977
23andMe	rs794727977
SNPshot	rs794727977
SNPdbe	rs794727977
MSV3d	rs794727977
GWAS Ctlg	rs794727977

Max Magnitude

0

ClinVar
Risk	rs794727977(T;T)
Alt	rs794727977(T;T)
Reference	Rs794727977(C;C)
Significance	Pathogenic
Disease	Mental retardation not provided
Variation	info
Gene	ARID1B
CLNDBN	Mental retardation, autosomal dominant 12 not provided
Reversed	0
HGVS	NC_000006.11:g.157469898C>T
CLNSRC
CLNACC	RCV000180674.1, RCV000358610.1,