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rs1060499774

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499774(G;T)
Make rs1060499774(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position66455465
GeneGRIP1
is asnp
is mentioned by
dbSNPrs1060499774
dbSNP (old)rs1060499774
ClinGenrs1060499774
ebirs1060499774
HLIrs1060499774
Exacrs1060499774
Gnomadrs1060499774
Varsomers1060499774
Maprs1060499774
PheGenIrs1060499774
Biobankrs1060499774
1000 genomesrs1060499774
hgdprs1060499774
ensemblrs1060499774
gopubmedrs1060499774
geneviewrs1060499774
scholarrs1060499774
googlers1060499774
pharmgkbrs1060499774
gwascentralrs1060499774
openSNPrs1060499774
23andMers1060499774
23andMe allrs1060499774
SNPshotrs1060499774
SNPdbers1060499774
MSV3drs1060499774
GWAS Ctlgrs1060499774
Max Magnitude0
ClinVar
Risk rs1060499774(T;T)
Alt rs1060499774(T;T)
Reference Rs1060499774(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene GRIP1
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000012.11:g.66849245C>A
CLNSRC
CLNACC RCV000454347.1,