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rs587784272

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587784272(G;G)
Make rs587784272(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2665395
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784272
ebirs587784272
HLIrs587784272
Exacrs587784272
Varsomers587784272
Maprs587784272
PheGenIrs587784272
hapmaprs587784272
1000 genomesrs587784272
hgdprs587784272
ensemblrs587784272
gopubmedrs587784272
geneviewrs587784272
scholarrs587784272
googlers587784272
pharmgkbrs587784272
gwascentralrs587784272
openSNPrs587784272
23andMers587784272
23andMe allrs587784272
SNP Nexus

SNPshotrs587784272
SNPdbers587784272
MSV3drs587784272
GWAS Ctlgrs587784272
Max Magnitude0
ClinVar
Risk rs587784272(G;G)
Alt rs587784272(G;G)
Reference rs587784272(T;T)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2568689T>G
CLNSRC
CLNACC RCV000147045.1,