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rs587784277

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784277(-;-)
Make rs587784277(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2672744
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784277
ebirs587784277
HLIrs587784277
Exacrs587784277
Varsomers587784277
Maprs587784277
PheGenIrs587784277
hapmaprs587784277
1000 genomesrs587784277
hgdprs587784277
ensemblrs587784277
gopubmedrs587784277
geneviewrs587784277
scholarrs587784277
googlers587784277
pharmgkbrs587784277
gwascentralrs587784277
openSNPrs587784277
23andMers587784277
23andMe allrs587784277
SNP Nexus

SNPshotrs587784277
SNPdbers587784277
MSV3drs587784277
GWAS Ctlgrs587784277
Max Magnitude0
ClinVar
Risk rs587784277(;)
Alt rs587784277(;)
Reference rs587784277(G;G)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2576038delG
CLNSRC
CLNACC RCV000147050.1,