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rs797045869

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs797045869(-;-)
Make rs797045869(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position2674159
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs797045869
dbSNP (old)rs797045869
ClinGenrs797045869
ebirs797045869
HLIrs797045869
Exacrs797045869
Varsomers797045869
Maprs797045869
PheGenIrs797045869
Biobankrs797045869
1000 genomesrs797045869
hgdprs797045869
ensemblrs797045869
gopubmedrs797045869
geneviewrs797045869
scholarrs797045869
googlers797045869
pharmgkbrs797045869
gwascentralrs797045869
openSNPrs797045869
23andMers797045869
23andMe allrs797045869
SNP Nexus

SNPshotrs797045869
SNPdbers797045869
MSV3drs797045869
GWAS Ctlgrs797045869
Max Magnitude0
ClinVar
Risk rs797045869(-;-)
Alt rs797045869(-;-)
Reference Rs797045869(TG;TG)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2577453_2577454delTG
CLNSRC
CLNACC RCV000194019.1,