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rs797045872

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045872(-;G)
Make rs797045872(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position2676537
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs797045872
dbSNP (old)rs797045872
ClinGenrs797045872
ebirs797045872
HLIrs797045872
Exacrs797045872
Varsomers797045872
Maprs797045872
PheGenIrs797045872
Biobankrs797045872
1000 genomesrs797045872
hgdprs797045872
ensemblrs797045872
gopubmedrs797045872
geneviewrs797045872
scholarrs797045872
googlers797045872
pharmgkbrs797045872
gwascentralrs797045872
openSNPrs797045872
23andMers797045872
23andMe allrs797045872
SNP Nexus

SNPshotrs797045872
SNPdbers797045872
MSV3drs797045872
GWAS Ctlgrs797045872
Max Magnitude0
ClinVar
Risk rs797045872(G;G)
Alt rs797045872(G;G)
Reference Rs797045872(-;-)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2579831dupG
CLNSRC
CLNACC RCV000193935.1,