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rs765815715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765815715(C;C)
Make rs765815715(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position61928394
GeneCDH4
is asnp
is mentioned by
dbSNPrs765815715
dbSNP (classic)rs765815715
ClinGenrs765815715
ebirs765815715
HLIrs765815715
Exacrs765815715
Gnomadrs765815715
Varsomers765815715
LitVarrs765815715
Maprs765815715
PheGenIrs765815715
Biobankrs765815715
1000 genomesrs765815715
hgdprs765815715
ensemblrs765815715
geneviewrs765815715
scholarrs765815715
googlers765815715
pharmgkbrs765815715
gwascentralrs765815715
openSNPrs765815715
23andMers765815715
SNPshotrs765815715
SNPdbers765815715
MSV3drs765815715
GWAS Ctlgrs765815715
Max Magnitude0
ClinVar
Risk rs765815715(A;A) rs765815715(C;C)
Alt rs765815715(A;A) rs765815715(C;C)
Reference Rs765815715(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene CDH4
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000020.10:g.60503452G>C
CLNSRC
CLNACC RCV000454293.1,