rs267607078

Orientation

plus

Stabilized

plus

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

Make rs267607078(C;T)

Make rs267607078(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

107634825

Gene

SOBP

is a	snp
is	mentioned by
dbSNP	rs267607078
dbSNP (classic)	rs267607078
ClinGen	rs267607078
ebi	rs267607078
HLI	rs267607078
Exac	rs267607078
Gnomad	rs267607078
Varsome	rs267607078
LitVar	rs267607078
Map	rs267607078
PheGenI	rs267607078
Biobank	rs267607078
1000 genomes	rs267607078
hgdp	rs267607078
ensembl	rs267607078
geneview	rs267607078
scholar	rs267607078
google	rs267607078
pharmgkb	rs267607078
gwascentral	rs267607078
openSNP	rs267607078
23andMe	rs267607078
SNPshot	rs267607078
SNPdbe	rs267607078
MSV3d	rs267607078
GWAS Ctlg	rs267607078

Max Magnitude

0

ClinVar
Risk	rs267607078(T;T)
Alt	rs267607078(T;T)
Reference	Rs267607078(C;C)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	SOBP
CLNDBN	Mental retardation, anterior maxillary protrusion, and strabismus
Reversed	0
HGVS	NC_000006.11:g.107956029C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000003.2,