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rs267607078

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607078(C;T)
Make rs267607078(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position107634825
GeneSOBP
is asnp
is mentioned by
dbSNPrs267607078
ebirs267607078
HLIrs267607078
Exacrs267607078
Varsomers267607078
Maprs267607078
PheGenIrs267607078
hapmaprs267607078
1000 genomesrs267607078
hgdprs267607078
ensemblrs267607078
gopubmedrs267607078
geneviewrs267607078
scholarrs267607078
googlers267607078
pharmgkbrs267607078
gwascentralrs267607078
openSNPrs267607078
23andMers267607078
23andMe allrs267607078
SNP Nexus

SNPshotrs267607078
SNPdbers267607078
MSV3drs267607078
GWAS Ctlgrs267607078
Max Magnitude0
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,