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rs1060499735

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499735(G;T)
Make rs1060499735(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position786584
GeneCPLX1, LOC105374339
is asnp
is mentioned by
dbSNPrs1060499735
dbSNP (old)rs1060499735
ClinGenrs1060499735
ebirs1060499735
HLIrs1060499735
Exacrs1060499735
Gnomadrs1060499735
Varsomers1060499735
Maprs1060499735
PheGenIrs1060499735
Biobankrs1060499735
1000 genomesrs1060499735
hgdprs1060499735
ensemblrs1060499735
gopubmedrs1060499735
geneviewrs1060499735
scholarrs1060499735
googlers1060499735
pharmgkbrs1060499735
gwascentralrs1060499735
openSNPrs1060499735
23andMers1060499735
23andMe allrs1060499735
SNPshotrs1060499735
SNPdbers1060499735
MSV3drs1060499735
GWAS Ctlgrs1060499735
Max Magnitude0
ClinVar
Risk rs1060499735(T;T)
Alt rs1060499735(T;T)
Reference Rs1060499735(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene CPLX1
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000004.11:g.780372C>A
CLNSRC
CLNACC RCV000454222.1,