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rs587777033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777033(C;G)
Make rs587777033(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position62361330
GeneKIF2A
is asnp
is mentioned by
dbSNPrs587777033
ebirs587777033
HLIrs587777033
Exacrs587777033
Varsomers587777033
Maprs587777033
PheGenIrs587777033
hapmaprs587777033
1000 genomesrs587777033
hgdprs587777033
ensemblrs587777033
gopubmedrs587777033
geneviewrs587777033
scholarrs587777033
googlers587777033
pharmgkbrs587777033
gwascentralrs587777033
openSNPrs587777033
23andMers587777033
23andMe allrs587777033
SNP Nexus

SNPshotrs587777033
SNPdbers587777033
MSV3drs587777033
GWAS Ctlgrs587777033
Max Magnitude0
ClinVar
Risk rs587777033(G;G)
Alt rs587777033(G;G)
Reference rs587777033(C;C)
Significance Pathogenic
Disease Cortical dysplasia
Variation info
Gene KIF2A
CLNDBN Cortical dysplasia, complex, with other brain malformations 3
Reversed 0
HGVS NC_000005.9:g.61657157C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000055623.2,