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rs730882061

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs730882061(-;-)
Make rs730882061(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position92616743
GeneKIF11
is asnp
is mentioned by
dbSNPrs730882061
ebirs730882061
HLIrs730882061
Exacrs730882061
Varsomers730882061
Maprs730882061
PheGenIrs730882061
hapmaprs730882061
1000 genomesrs730882061
hgdprs730882061
ensemblrs730882061
gopubmedrs730882061
geneviewrs730882061
scholarrs730882061
googlers730882061
pharmgkbrs730882061
gwascentralrs730882061
openSNPrs730882061
23andMers730882061
23andMe allrs730882061
SNP Nexus

SNPshotrs730882061
SNPdbers730882061
MSV3drs730882061
GWAS Ctlgrs730882061
Max Magnitude0
ClinVar
Risk rs730882061(;)
Alt rs730882061(;)
Reference rs730882061(CT;CT)
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.94376500_94376501delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000022635.26,