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rs587784290

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784290(A;A)
Make rs587784290(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2674289
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784290
ebirs587784290
HLIrs587784290
Exacrs587784290
Varsomers587784290
Maprs587784290
PheGenIrs587784290
hapmaprs587784290
1000 genomesrs587784290
hgdprs587784290
ensemblrs587784290
gopubmedrs587784290
geneviewrs587784290
scholarrs587784290
googlers587784290
pharmgkbrs587784290
gwascentralrs587784290
openSNPrs587784290
23andMers587784290
23andMe allrs587784290
SNP Nexus

SNPshotrs587784290
SNPdbers587784290
MSV3drs587784290
GWAS Ctlgrs587784290
Max Magnitude0
ClinVar
Risk rs587784290(A;A)
Alt rs587784290(A;A)
Reference rs587784290(G;G)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2577583G>A
CLNSRC
CLNACC RCV000147066.1,