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rs587784250

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784250(A;A)
Make rs587784250(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2666019
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784250
ebirs587784250
HLIrs587784250
Exacrs587784250
Varsomers587784250
Maprs587784250
PheGenIrs587784250
hapmaprs587784250
1000 genomesrs587784250
hgdprs587784250
ensemblrs587784250
gopubmedrs587784250
geneviewrs587784250
scholarrs587784250
googlers587784250
pharmgkbrs587784250
gwascentralrs587784250
openSNPrs587784250
23andMers587784250
23andMe allrs587784250
SNP Nexus

SNPshotrs587784250
SNPdbers587784250
MSV3drs587784250
GWAS Ctlgrs587784250
Max Magnitude0
ClinVar
Risk rs587784250(A;A)
Alt rs587784250(A;A)
Reference rs587784250(G;G)
Significance Probable-Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2569313G>A
CLNSRC
CLNACC RCV000147019.1,