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rs587784266

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784266(A;A)
Make rs587784266(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2670168
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784266
ebirs587784266
HLIrs587784266
Exacrs587784266
Varsomers587784266
Maprs587784266
PheGenIrs587784266
hapmaprs587784266
1000 genomesrs587784266
hgdprs587784266
ensemblrs587784266
gopubmedrs587784266
geneviewrs587784266
scholarrs587784266
googlers587784266
pharmgkbrs587784266
gwascentralrs587784266
openSNPrs587784266
23andMers587784266
23andMe allrs587784266
SNP Nexus

SNPshotrs587784266
SNPdbers587784266
MSV3drs587784266
GWAS Ctlgrs587784266
Max Magnitude0
ClinVar
Risk rs587784266(A;A)
Alt rs587784266(A;A)
Reference rs587784266(G;G)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2573462G>A
CLNSRC
CLNACC RCV000147037.1,