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rs369384363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369384363(A;A)
Make rs369384363(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position91338121
GeneCCDC88C
is asnp
is mentioned by
dbSNPrs369384363
ebirs369384363
HLIrs369384363
Exacrs369384363
Varsomers369384363
Maprs369384363
PheGenIrs369384363
hapmaprs369384363
1000 genomesrs369384363
hgdprs369384363
ensemblrs369384363
gopubmedrs369384363
geneviewrs369384363
scholarrs369384363
googlers369384363
pharmgkbrs369384363
gwascentralrs369384363
openSNPrs369384363
23andMers369384363
23andMe allrs369384363
SNP Nexus

SNPshotrs369384363
SNPdbers369384363
MSV3drs369384363
GWAS Ctlgrs369384363
Max Magnitude0
ClinVar
Risk rs369384363(A,C;A,C)
Alt rs369384363(A,C;A,C)
Reference rs369384363(G;G)
Significance Pathogenic
Disease Hydrocephalus
Variation info
Gene CCDC88C
CLNDBN Hydrocephalus
Reversed 0
HGVS NC_000014.8:g.91804465G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000033088.4,