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

rs587784263

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587784263(A;T)
Make rs587784263(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2667185
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784263
ebirs587784263
HLIrs587784263
Exacrs587784263
Varsomers587784263
Maprs587784263
PheGenIrs587784263
hapmaprs587784263
1000 genomesrs587784263
hgdprs587784263
ensemblrs587784263
gopubmedrs587784263
geneviewrs587784263
scholarrs587784263
googlers587784263
pharmgkbrs587784263
gwascentralrs587784263
openSNPrs587784263
23andMers587784263
23andMe allrs587784263
SNP Nexus

SNPshotrs587784263
SNPdbers587784263
MSV3drs587784263
GWAS Ctlgrs587784263
Max Magnitude0
ClinVar
Risk rs587784263(T;T)
Alt rs587784263(T;T)
Reference rs587784263(A;A)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2570479A>T
CLNSRC
CLNACC RCV000147033.1,