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rs587784239

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784239(A;A)
Make rs587784239(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2680225
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784239
ebirs587784239
HLIrs587784239
Exacrs587784239
Varsomers587784239
Maprs587784239
PheGenIrs587784239
hapmaprs587784239
1000 genomesrs587784239
hgdprs587784239
ensemblrs587784239
gopubmedrs587784239
geneviewrs587784239
scholarrs587784239
googlers587784239
pharmgkbrs587784239
gwascentralrs587784239
openSNPrs587784239
23andMers587784239
23andMe allrs587784239
SNP Nexus

SNPshotrs587784239
SNPdbers587784239
MSV3drs587784239
GWAS Ctlgrs587784239
Max Magnitude0
ClinVar
Risk rs587784239(A;A)
Alt rs587784239(A;A)
Reference rs587784239(G;G)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2583519G>A
CLNSRC
CLNACC RCV000147008.1,