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rs387906641

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906641(C;T)
Make rs387906641(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position92621415
GeneKIF11
is asnp
is mentioned by
dbSNPrs387906641
ebirs387906641
HLIrs387906641
Exacrs387906641
Varsomers387906641
Maprs387906641
PheGenIrs387906641
hapmaprs387906641
1000 genomesrs387906641
hgdprs387906641
ensemblrs387906641
gopubmedrs387906641
geneviewrs387906641
scholarrs387906641
googlers387906641
pharmgkbrs387906641
gwascentralrs387906641
openSNPrs387906641
23andMers387906641
23andMe allrs387906641
SNP Nexus

SNPshotrs387906641
SNPdbers387906641
MSV3drs387906641
GWAS Ctlgrs387906641
Max Magnitude0
ClinVar
Risk rs387906641(T;T)
Alt rs387906641(T;T)
Reference rs387906641(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.94381172C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022634.23,