rs387907141

Orientation

plus

Stabilized

plus

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

Make rs387907141(C;T)

Make rs387907141(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

157181137

Gene

ARID1B

is a	snp
is	mentioned by
dbSNP	rs387907141
dbSNP (classic)	rs387907141
ClinGen	rs387907141
ebi	rs387907141
HLI	rs387907141
Exac	rs387907141
Gnomad	rs387907141
Varsome	rs387907141
LitVar	rs387907141
Map	rs387907141
PheGenI	rs387907141
Biobank	rs387907141
1000 genomes	rs387907141
hgdp	rs387907141
ensembl	rs387907141
geneview	rs387907141
scholar	rs387907141
google	rs387907141
pharmgkb	rs387907141
gwascentral	rs387907141
openSNP	rs387907141
23andMe	rs387907141
SNPshot	rs387907141
SNPdbe	rs387907141
MSV3d	rs387907141
GWAS Ctlg	rs387907141

Max Magnitude

0

ClinVar
Risk	rs387907141(T;T)
Alt	rs387907141(T;T)
Reference	Rs387907141(C;C)
Significance	Pathogenic
Disease	Coffin-Siris syndrome 1 not provided
Variation	info
Gene	ARID1B
CLNDBN	Coffin-Siris syndrome 1 not provided
Reversed	0
HGVS	NC_000006.11:g.157502271C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024209.3, RCV000254764.1,