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rs587777570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777570(A;A)
Make rs587777570(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
is asnp
is mentioned by
dbSNPrs587777570
ebirs587777570
HLIrs587777570
Exacrs587777570
Varsomers587777570
Maprs587777570
PheGenIrs587777570
hapmaprs587777570
1000 genomesrs587777570
hgdprs587777570
ensemblrs587777570
gopubmedrs587777570
geneviewrs587777570
scholarrs587777570
googlers587777570
pharmgkbrs587777570
gwascentralrs587777570
openSNPrs587777570
23andMers587777570
23andMe allrs587777570
SNP Nexus

SNPshotrs587777570
SNPdbers587777570
MSV3drs587777570
GWAS Ctlgrs587777570
Max Magnitude0
ClinVar
Risk rs587777570(A;A)
Alt rs587777570(A;A)
Reference rs587777570(G;G)
Significance Pathogenic
Disease Cortical dysplasia
Variation info
Gene KIF5C
CLNDBN Cortical dysplasia, complex, with other brain malformations 2
Reversed 0
HGVS NC_000002.11:g.149803532G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128852.2,