Have questions? Visit https://www.reddit.com/r/SNPedia

rs587784264

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784264(A;A)
Make rs587784264(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2667199
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784264
ebirs587784264
HLIrs587784264
Exacrs587784264
Varsomers587784264
Maprs587784264
PheGenIrs587784264
hapmaprs587784264
1000 genomesrs587784264
hgdprs587784264
ensemblrs587784264
gopubmedrs587784264
geneviewrs587784264
scholarrs587784264
googlers587784264
pharmgkbrs587784264
gwascentralrs587784264
openSNPrs587784264
23andMers587784264
23andMe allrs587784264
SNP Nexus

SNPshotrs587784264
SNPdbers587784264
MSV3drs587784264
GWAS Ctlgrs587784264
Max Magnitude0
ClinVar
Risk rs587784264(A;A)
Alt rs587784264(A;A)
Reference rs587784264(G;G)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2570493G>A
CLNSRC
CLNACC RCV000147035.1,