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rs587784291

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784291(A;A)
Make rs587784291(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2674288
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784291
ebirs587784291
HLIrs587784291
Exacrs587784291
Varsomers587784291
Maprs587784291
PheGenIrs587784291
hapmaprs587784291
1000 genomesrs587784291
hgdprs587784291
ensemblrs587784291
gopubmedrs587784291
geneviewrs587784291
scholarrs587784291
googlers587784291
pharmgkbrs587784291
gwascentralrs587784291
openSNPrs587784291
23andMers587784291
23andMe allrs587784291
SNP Nexus

SNPshotrs587784291
SNPdbers587784291
MSV3drs587784291
GWAS Ctlgrs587784291
Max Magnitude0
ClinVar
Risk rs587784291(A;A)
Alt rs587784291(A;A)
Reference rs587784291(G;G)
Significance Probable-Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2577582G>A
CLNSRC
CLNACC RCV000147067.1,