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

rs587784237

From SNPedia

Orientationplus
Geno Mag Summary
(CGTGGAGT;CGTGGAGT) 0 common in clinvar
Make rs587784237(-;-)
Make rs587784237(-;CGTGGAGT)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2680185
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784237
ebirs587784237
HLIrs587784237
Exacrs587784237
Varsomers587784237
Maprs587784237
PheGenIrs587784237
hapmaprs587784237
1000 genomesrs587784237
hgdprs587784237
ensemblrs587784237
gopubmedrs587784237
geneviewrs587784237
scholarrs587784237
googlers587784237
pharmgkbrs587784237
gwascentralrs587784237
openSNPrs587784237
23andMers587784237
23andMe allrs587784237
SNP Nexus

SNPshotrs587784237
SNPdbers587784237
MSV3drs587784237
GWAS Ctlgrs587784237
Max Magnitude0
ClinVar
Risk rs587784237(;)
Alt rs587784237(;)
Reference rs587784237(CGTGGAGT;CGTGGAGT)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2583479_2583486delCGTGGAGT
CLNSRC
CLNACC RCV000147006.1,