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rs797045856

From SNPedia

Merged intors113994201
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045856(-;G)
Make rs797045856(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position2680206
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs797045856
ClinGenrs797045856
ebirs797045856
HLIrs797045856
Exacrs797045856
Varsomers797045856
Maprs797045856
PheGenIrs797045856
hapmaprs797045856
1000 genomesrs797045856
hgdprs797045856
ensemblrs797045856
gopubmedrs797045856
geneviewrs797045856
scholarrs797045856
googlers797045856
pharmgkbrs797045856
gwascentralrs797045856
openSNPrs797045856
23andMers797045856
23andMe allrs797045856
SNP Nexus

SNPshotrs797045856
SNPdbers797045856
MSV3drs797045856
GWAS Ctlgrs797045856
StatusMerged into rs113994201
Max Magnitude0
ClinVar
Risk rs797045856(G;G)
Alt rs797045856(G;G)
Reference Rs797045856(;)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2583505dupG
CLNSRC
CLNACC RCV000020299.3,