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rs587784236

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784236(C;G)
Make rs587784236(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2680170
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784236
ebirs587784236
HLIrs587784236
Exacrs587784236
Varsomers587784236
Maprs587784236
PheGenIrs587784236
hapmaprs587784236
1000 genomesrs587784236
hgdprs587784236
ensemblrs587784236
gopubmedrs587784236
geneviewrs587784236
scholarrs587784236
googlers587784236
pharmgkbrs587784236
gwascentralrs587784236
openSNPrs587784236
23andMers587784236
23andMe allrs587784236
SNP Nexus

SNPshotrs587784236
SNPdbers587784236
MSV3drs587784236
GWAS Ctlgrs587784236
Max Magnitude0
ClinVar
Risk rs587784236(G,T;G,T)
Alt rs587784236(G,T;G,T)
Reference rs587784236(C;C)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2583464C>G; NC_000017.10:g.2583464C>T
CLNSRC
CLNACC RCV000147004.1, RCV000147005.1,