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rs387907321

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs387907321(-;-)
Make rs387907321(-;AG)
ReferenceGRCh38 38.1/141
Chromosome14
Position91272870
GeneCCDC88C
is asnp
is mentioned by
dbSNPrs387907321
ebirs387907321
HLIrs387907321
Exacrs387907321
Varsomers387907321
Maprs387907321
PheGenIrs387907321
hapmaprs387907321
1000 genomesrs387907321
hgdprs387907321
ensemblrs387907321
gopubmedrs387907321
geneviewrs387907321
scholarrs387907321
googlers387907321
pharmgkbrs387907321
gwascentralrs387907321
openSNPrs387907321
23andMers387907321
23andMe allrs387907321
SNP Nexus

SNPshotrs387907321
SNPdbers387907321
MSV3drs387907321
GWAS Ctlgrs387907321
Max Magnitude0
ClinVar
Risk rs387907321(;)
Alt rs387907321(;)
Reference rs387907321(AG;AG)
Significance Pathogenic
Disease Hydrocephalus
Variation info
Gene CCDC88C
CLNDBN Hydrocephalus
Reversed 1
HGVS NC_000014.8:g.91739214_91739215delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000033089.5,