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rs797045855

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045855(-;T)
Make rs797045855(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position2680179
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs797045855
ClinGenrs797045855
ebirs797045855
HLIrs797045855
Exacrs797045855
Varsomers797045855
Maprs797045855
PheGenIrs797045855
hapmaprs797045855
1000 genomesrs797045855
hgdprs797045855
ensemblrs797045855
gopubmedrs797045855
geneviewrs797045855
scholarrs797045855
googlers797045855
pharmgkbrs797045855
gwascentralrs797045855
openSNPrs797045855
23andMers797045855
23andMe allrs797045855
SNP Nexus

SNPshotrs797045855
SNPdbers797045855
MSV3drs797045855
GWAS Ctlgrs797045855
Max Magnitude0
ClinVar
Risk rs797045855(T;T)
Alt rs797045855(T;T)
Reference Rs797045855(;)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2583473dupT
CLNSRC
CLNACC RCV000194197.1,