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rs587784287

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587784287(A;C)
Make rs587784287(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2674139
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784287
ebirs587784287
HLIrs587784287
Exacrs587784287
Varsomers587784287
Maprs587784287
PheGenIrs587784287
hapmaprs587784287
1000 genomesrs587784287
hgdprs587784287
ensemblrs587784287
gopubmedrs587784287
geneviewrs587784287
scholarrs587784287
googlers587784287
pharmgkbrs587784287
gwascentralrs587784287
openSNPrs587784287
23andMers587784287
23andMe allrs587784287
SNP Nexus

SNPshotrs587784287
SNPdbers587784287
MSV3drs587784287
GWAS Ctlgrs587784287
Max Magnitude0
ClinVar
Risk rs587784287(C;C)
Alt rs587784287(C;C)
Reference rs587784287(A;A)
Significance Probable-Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2577433A>C
CLNSRC
CLNACC RCV000147061.1,