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rs797045862

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045862(-;T)
Make rs797045862(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position2670300
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs797045862
ClinGenrs797045862
ebirs797045862
HLIrs797045862
Exacrs797045862
Varsomers797045862
Maprs797045862
PheGenIrs797045862
hapmaprs797045862
1000 genomesrs797045862
hgdprs797045862
ensemblrs797045862
gopubmedrs797045862
geneviewrs797045862
scholarrs797045862
googlers797045862
pharmgkbrs797045862
gwascentralrs797045862
openSNPrs797045862
23andMers797045862
23andMe allrs797045862
SNP Nexus

SNPshotrs797045862
SNPdbers797045862
MSV3drs797045862
GWAS Ctlgrs797045862
Max Magnitude0
ClinVar
Risk rs797045862(T;T)
Alt rs797045862(T;T)
Reference Rs797045862(;)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2573594dupT
CLNSRC
CLNACC RCV000192553.1,