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rs387906643

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906643(C;G)
Make rs387906643(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position92613045
GeneKIF11
is asnp
is mentioned by
dbSNPrs387906643
ebirs387906643
HLIrs387906643
Exacrs387906643
Varsomers387906643
Maprs387906643
PheGenIrs387906643
hapmaprs387906643
1000 genomesrs387906643
hgdprs387906643
ensemblrs387906643
gopubmedrs387906643
geneviewrs387906643
scholarrs387906643
googlers387906643
pharmgkbrs387906643
gwascentralrs387906643
openSNPrs387906643
23andMers387906643
23andMe allrs387906643
SNP Nexus

SNPshotrs387906643
SNPdbers387906643
MSV3drs387906643
GWAS Ctlgrs387906643
Max Magnitude0
ClinVar
Risk rs387906643(G;G)
Alt rs387906643(G;G)
Reference rs387906643(C;C)
Significance Pathogenic
Disease Microcephaly with or without chorioretinopathy
Variation info
Gene KIF11
CLNDBN Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
Reversed 0
HGVS NC_000010.10:g.94372802C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022639.22,