rs869312712

Orientation

plus

Stabilized

plus

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

Make rs869312712(C;T)

Make rs869312712(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

6

Position

157084866

Gene

ARID1B

is a	snp
is	mentioned by
dbSNP	rs869312712
dbSNP (classic)	rs869312712
ClinGen	rs869312712
ebi	rs869312712
HLI	rs869312712
Exac	rs869312712
Gnomad	rs869312712
Varsome	rs869312712
LitVar	rs869312712
Map	rs869312712
PheGenI	rs869312712
Biobank	rs869312712
1000 genomes	rs869312712
hgdp	rs869312712
ensembl	rs869312712
geneview	rs869312712
scholar	rs869312712
google	rs869312712
pharmgkb	rs869312712
gwascentral	rs869312712
openSNP	rs869312712
23andMe	rs869312712
SNPshot	rs869312712
SNPdbe	rs869312712
MSV3d	rs869312712
GWAS Ctlg	rs869312712

Max Magnitude

0

ClinVar
Risk	rs869312712(T;T)
Alt	rs869312712(T;T)
Reference	Rs869312712(C;C)
Significance	Pathogenic
Disease	Coffin-Siris syndrome 1
Variation	info
Gene	ARID1B
CLNDBN	Coffin-Siris syndrome 1
Reversed	0
HGVS	NC_000006.11:g.157406000C>T
CLNSRC
CLNACC	RCV000209876.1,