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rs587784258

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784258(C;T)
Make rs587784258(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2667064
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784258
ebirs587784258
HLIrs587784258
Exacrs587784258
Varsomers587784258
Maprs587784258
PheGenIrs587784258
hapmaprs587784258
1000 genomesrs587784258
hgdprs587784258
ensemblrs587784258
gopubmedrs587784258
geneviewrs587784258
scholarrs587784258
googlers587784258
pharmgkbrs587784258
gwascentralrs587784258
openSNPrs587784258
23andMers587784258
23andMe allrs587784258
SNP Nexus

SNPshotrs587784258
SNPdbers587784258
MSV3drs587784258
GWAS Ctlgrs587784258
Max Magnitude0
ClinVar
Risk rs587784258(T;T)
Alt rs587784258(T;T)
Reference rs587784258(C;C)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2570358C>T
CLNSRC
CLNACC RCV000147028.1,