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rs786205900

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205900(G;T)
Make rs786205900(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position92630278
GeneKIF11
is asnp
is mentioned by
dbSNPrs786205900
ebirs786205900
HLIrs786205900
Exacrs786205900
Varsomers786205900
Maprs786205900
PheGenIrs786205900
hapmaprs786205900
1000 genomesrs786205900
hgdprs786205900
ensemblrs786205900
gopubmedrs786205900
geneviewrs786205900
scholarrs786205900
googlers786205900
pharmgkbrs786205900
gwascentralrs786205900
openSNPrs786205900
23andMers786205900
23andMe allrs786205900
SNP Nexus

SNPshotrs786205900
SNPdbers786205900
MSV3drs786205900
GWAS Ctlgrs786205900
Max Magnitude0
ClinVar
Risk rs786205900(T;T)
Alt rs786205900(T;T)
Reference rs786205900(G;G)
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.94390035G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000172876.2,