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

rs587784286

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784286(C;T)
Make rs587784286(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2674118
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784286
ebirs587784286
HLIrs587784286
Exacrs587784286
Varsomers587784286
Maprs587784286
PheGenIrs587784286
hapmaprs587784286
1000 genomesrs587784286
hgdprs587784286
ensemblrs587784286
gopubmedrs587784286
geneviewrs587784286
scholarrs587784286
googlers587784286
pharmgkbrs587784286
gwascentralrs587784286
openSNPrs587784286
23andMers587784286
23andMe allrs587784286
SNP Nexus

SNPshotrs587784286
SNPdbers587784286
MSV3drs587784286
GWAS Ctlgrs587784286
Max Magnitude0
ClinVar
Risk rs587784286(T;T)
Alt rs587784286(T;T)
Reference rs587784286(C;C)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2577412C>T
CLNSRC
CLNACC RCV000147060.1,