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

rs587784256

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784256(A;A)
Make rs587784256(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2666091
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784256
ebirs587784256
HLIrs587784256
Exacrs587784256
Varsomers587784256
Maprs587784256
PheGenIrs587784256
hapmaprs587784256
1000 genomesrs587784256
hgdprs587784256
ensemblrs587784256
gopubmedrs587784256
geneviewrs587784256
scholarrs587784256
googlers587784256
pharmgkbrs587784256
gwascentralrs587784256
openSNPrs587784256
23andMers587784256
23andMe allrs587784256
SNP Nexus

SNPshotrs587784256
SNPdbers587784256
MSV3drs587784256
GWAS Ctlgrs587784256
Max Magnitude0
ClinVar
Risk rs587784256(A,T;A,T)
Alt rs587784256(A,T;A,T)
Reference rs587784256(G;G)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2569385G>A; NC_000017.10:g.2569385G>T
CLNSRC
CLNACC RCV000147025.1, RCV000147026.1,