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

rs797045864

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045864(-;A)
Make rs797045864(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position2672753
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs797045864
ClinGenrs797045864
ebirs797045864
HLIrs797045864
Exacrs797045864
Varsomers797045864
Maprs797045864
PheGenIrs797045864
hapmaprs797045864
1000 genomesrs797045864
hgdprs797045864
ensemblrs797045864
gopubmedrs797045864
geneviewrs797045864
scholarrs797045864
googlers797045864
pharmgkbrs797045864
gwascentralrs797045864
openSNPrs797045864
23andMers797045864
23andMe allrs797045864
SNP Nexus

SNPshotrs797045864
SNPdbers797045864
MSV3drs797045864
GWAS Ctlgrs797045864
Max Magnitude0
ClinVar
Risk rs797045864(A;A)
Alt rs797045864(A;A)
Reference Rs797045864(-;-)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2576047dupA
CLNSRC
CLNACC RCV000194642.1,