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rs587784261

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587784261(A;A)
Make rs587784261(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position2667170
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs587784261
ebirs587784261
HLIrs587784261
Exacrs587784261
Varsomers587784261
Maprs587784261
PheGenIrs587784261
hapmaprs587784261
1000 genomesrs587784261
hgdprs587784261
ensemblrs587784261
gopubmedrs587784261
geneviewrs587784261
scholarrs587784261
googlers587784261
pharmgkbrs587784261
gwascentralrs587784261
openSNPrs587784261
23andMers587784261
23andMe allrs587784261
SNP Nexus

SNPshotrs587784261
SNPdbers587784261
MSV3drs587784261
GWAS Ctlgrs587784261
Max Magnitude0
ClinVar
Risk rs587784261(A;A)
Alt rs587784261(A;A)
Reference rs587784261(T;T)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2570464T>A
CLNSRC
CLNACC RCV000147031.1,