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rs387907320

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907320(A;A)
Make rs387907320(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position91277921
GeneCCDC88C
is asnp
is mentioned by
dbSNPrs387907320
ebirs387907320
HLIrs387907320
Exacrs387907320
Varsomers387907320
Maprs387907320
PheGenIrs387907320
hapmaprs387907320
1000 genomesrs387907320
hgdprs387907320
ensemblrs387907320
gopubmedrs387907320
geneviewrs387907320
scholarrs387907320
googlers387907320
pharmgkbrs387907320
gwascentralrs387907320
openSNPrs387907320
23andMers387907320
23andMe allrs387907320
SNP Nexus

SNPshotrs387907320
SNPdbers387907320
MSV3drs387907320
GWAS Ctlgrs387907320
Max Magnitude0
ClinVar
Risk rs387907320(A;A)
Alt rs387907320(A;A)
Reference rs387907320(G;G)
Significance Pathogenic
Disease Hydrocephalus
Variation info
Gene CCDC88C
CLNDBN Hydrocephalus
Reversed 1
HGVS NC_000014.8:g.91744265C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033087.5,