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rs797045866

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045866(-;AT)
Make rs797045866(AT;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position2665411
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs797045866
ClinGenrs797045866
ebirs797045866
HLIrs797045866
Exacrs797045866
Varsomers797045866
Maprs797045866
PheGenIrs797045866
hapmaprs797045866
1000 genomesrs797045866
hgdprs797045866
ensemblrs797045866
gopubmedrs797045866
geneviewrs797045866
scholarrs797045866
googlers797045866
pharmgkbrs797045866
gwascentralrs797045866
openSNPrs797045866
23andMers797045866
23andMe allrs797045866
SNP Nexus

SNPshotrs797045866
SNPdbers797045866
MSV3drs797045866
GWAS Ctlgrs797045866
Max Magnitude0
ClinVar
Risk rs797045866(TA;TA)
Alt rs797045866(TA;TA)
Reference Rs797045866(;)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2568704_2568705dupAT
CLNSRC
CLNACC RCV000194082.1,