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rs587784262

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784262(C;T)
Make rs587784262(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2665376
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784262
ebirs587784262
HLIrs587784262
Exacrs587784262
Varsomers587784262
Maprs587784262
PheGenIrs587784262
hapmaprs587784262
1000 genomesrs587784262
hgdprs587784262
ensemblrs587784262
gopubmedrs587784262
geneviewrs587784262
scholarrs587784262
googlers587784262
pharmgkbrs587784262
gwascentralrs587784262
openSNPrs587784262
23andMers587784262
23andMe allrs587784262
SNP Nexus

SNPshotrs587784262
SNPdbers587784262
MSV3drs587784262
GWAS Ctlgrs587784262
Max Magnitude0
ClinVar
Risk rs587784262(T;T)
Alt rs587784262(T;T)
Reference rs587784262(C;C)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2568670C>T
CLNSRC
CLNACC RCV000147032.1,