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rs794729199

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729199(A;A)
Make rs794729199(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position2674206
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs794729199
ebirs794729199
HLIrs794729199
Exacrs794729199
Varsomers794729199
Maprs794729199
PheGenIrs794729199
hapmaprs794729199
1000 genomesrs794729199
hgdprs794729199
ensemblrs794729199
gopubmedrs794729199
geneviewrs794729199
scholarrs794729199
googlers794729199
pharmgkbrs794729199
gwascentralrs794729199
openSNPrs794729199
23andMers794729199
23andMe allrs794729199
SNP Nexus

SNPshotrs794729199
SNPdbers794729199
MSV3drs794729199
GWAS Ctlgrs794729199
Max Magnitude0
ClinVar
Risk rs794729199(A;A)
Alt rs794729199(A;A)
Reference rs794729199(G;G)
Significance Probable-Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2577500G>A
CLNSRC
CLNACC RCV000184018.1,