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rs199768740

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199768740(C;T)
Make rs199768740(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position66541927
GeneGRIP1
is asnp
is mentioned by
dbSNPrs199768740
dbSNP (old)rs199768740
ClinGenrs199768740
ebirs199768740
HLIrs199768740
Exacrs199768740
Gnomadrs199768740
Varsomers199768740
Maprs199768740
PheGenIrs199768740
Biobankrs199768740
1000 genomesrs199768740
hgdprs199768740
ensemblrs199768740
gopubmedrs199768740
geneviewrs199768740
scholarrs199768740
googlers199768740
pharmgkbrs199768740
gwascentralrs199768740
openSNPrs199768740
23andMers199768740
23andMe allrs199768740
SNPshotrs199768740
SNPdbers199768740
MSV3drs199768740
GWAS Ctlgrs199768740
Max Magnitude0
ClinVar
Risk rs199768740(T;T)
Alt rs199768740(T;T)
Reference Rs199768740(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene GRIP1
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000012.11:g.66935707C>T
CLNSRC
CLNACC RCV000454212.1,