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rs587784265

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784265(A;A)
Make rs587784265(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2638291
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784265
ebirs587784265
HLIrs587784265
Exacrs587784265
Varsomers587784265
Maprs587784265
PheGenIrs587784265
hapmaprs587784265
1000 genomesrs587784265
hgdprs587784265
ensemblrs587784265
gopubmedrs587784265
geneviewrs587784265
scholarrs587784265
googlers587784265
pharmgkbrs587784265
gwascentralrs587784265
openSNPrs587784265
23andMers587784265
23andMe allrs587784265
SNP Nexus

SNPshotrs587784265
SNPdbers587784265
MSV3drs587784265
GWAS Ctlgrs587784265
Max Magnitude0
ClinVar
Risk rs587784265(A;A)
Alt rs587784265(A;A)
Reference rs587784265(G;G)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2541585G>A
CLNSRC
CLNACC RCV000147036.1,