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rs730882062

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730882062(-;-)
Make rs730882062(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position92632583
GeneKIF11
is asnp
is mentioned by
dbSNPrs730882062
ebirs730882062
HLIrs730882062
Exacrs730882062
Varsomers730882062
Maprs730882062
PheGenIrs730882062
hapmaprs730882062
1000 genomesrs730882062
hgdprs730882062
ensemblrs730882062
gopubmedrs730882062
geneviewrs730882062
scholarrs730882062
googlers730882062
pharmgkbrs730882062
gwascentralrs730882062
openSNPrs730882062
23andMers730882062
23andMe allrs730882062
SNP Nexus

SNPshotrs730882062
SNPdbers730882062
MSV3drs730882062
GWAS Ctlgrs730882062
Max Magnitude0
ClinVar
Risk rs730882062(;)
Alt rs730882062(;)
Reference rs730882062(A;A)
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.94392340delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000022637.26,