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rs369259961

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs369259961(C;C)
Make rs369259961(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position2665423
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs369259961
ebirs369259961
HLIrs369259961
Exacrs369259961
Varsomers369259961
Maprs369259961
PheGenIrs369259961
hapmaprs369259961
1000 genomesrs369259961
hgdprs369259961
ensemblrs369259961
gopubmedrs369259961
geneviewrs369259961
scholarrs369259961
googlers369259961
pharmgkbrs369259961
gwascentralrs369259961
openSNPrs369259961
23andMers369259961
23andMe allrs369259961
SNP Nexus

SNPshotrs369259961
SNPdbers369259961
MSV3drs369259961
GWAS Ctlgrs369259961
Max Magnitude0
ClinVar
Risk rs369259961(C,G;C,G)
Alt rs369259961(C,G;C,G)
Reference rs369259961(T;T)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2568717T>G
CLNSRC ClinVar University of Chicago
CLNACC RCV000147064.1,