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rs587783867

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783867(C;T)
Make rs587783867(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position15691243
GeneNDE1
is asnp
is mentioned by
dbSNPrs587783867
ebirs587783867
HLIrs587783867
Exacrs587783867
Varsomers587783867
Maprs587783867
PheGenIrs587783867
hapmaprs587783867
1000 genomesrs587783867
hgdprs587783867
ensemblrs587783867
gopubmedrs587783867
geneviewrs587783867
scholarrs587783867
googlers587783867
pharmgkbrs587783867
gwascentralrs587783867
openSNPrs587783867
23andMers587783867
23andMe allrs587783867
SNP Nexus

SNPshotrs587783867
SNPdbers587783867
MSV3drs587783867
GWAS Ctlgrs587783867
Max Magnitude0
ClinVar
Risk rs587783867(T;T)
Alt rs587783867(T;T)
Reference rs587783867(C;C)
Significance Probable-Pathogenic
Disease Lissencephaly 4 not provided
Variation info
Gene NDE1
CLNDBN Lissencephaly 4 not provided
Reversed 0
HGVS NC_000016.9:g.15785100C>T
CLNSRC
CLNACC RCV000146495.1, RCV000171245.1,