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rs1060499765

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499765(A;A)
Make rs1060499765(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position8737163
GenePLCB1
is asnp
is mentioned by
dbSNPrs1060499765
dbSNP (old)rs1060499765
ClinGenrs1060499765
ebirs1060499765
HLIrs1060499765
Exacrs1060499765
Gnomadrs1060499765
Varsomers1060499765
Maprs1060499765
PheGenIrs1060499765
Biobankrs1060499765
1000 genomesrs1060499765
hgdprs1060499765
ensemblrs1060499765
gopubmedrs1060499765
geneviewrs1060499765
scholarrs1060499765
googlers1060499765
pharmgkbrs1060499765
gwascentralrs1060499765
openSNPrs1060499765
23andMers1060499765
23andMe allrs1060499765
SNPshotrs1060499765
SNPdbers1060499765
MSV3drs1060499765
GWAS Ctlgrs1060499765
Max Magnitude0
ClinVar
Risk rs1060499765(A;A)
Alt rs1060499765(A;A)
Reference Rs1060499765(T;T)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene PLCB1
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000020.10:g.8717810T>A
CLNSRC
CLNACC RCV000454325.1,