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rs797045859

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045859(-;T)
Make rs797045859(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position2667146
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs797045859
dbSNP (old)rs797045859
ClinGenrs797045859
ebirs797045859
HLIrs797045859
Exacrs797045859
Gnomadrs797045859
Varsomers797045859
Maprs797045859
PheGenIrs797045859
Biobankrs797045859
1000 genomesrs797045859
hgdprs797045859
ensemblrs797045859
gopubmedrs797045859
geneviewrs797045859
scholarrs797045859
googlers797045859
pharmgkbrs797045859
gwascentralrs797045859
openSNPrs797045859
23andMers797045859
23andMe allrs797045859
SNP Nexus

SNPshotrs797045859
SNPdbers797045859
MSV3drs797045859
GWAS Ctlgrs797045859
Max Magnitude0
ClinVar
Risk rs797045859(T;T)
Alt rs797045859(T;T)
Reference Rs797045859(-;-)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2570440dupT
CLNSRC
CLNACC RCV000192650.1,