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rs797045061

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045061(A;T)
Make rs797045061(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position2670286
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs797045061
ebirs797045061
HLIrs797045061
Exacrs797045061
Varsomers797045061
Maprs797045061
PheGenIrs797045061
hapmaprs797045061
1000 genomesrs797045061
hgdprs797045061
ensemblrs797045061
gopubmedrs797045061
geneviewrs797045061
scholarrs797045061
googlers797045061
pharmgkbrs797045061
gwascentralrs797045061
openSNPrs797045061
23andMers797045061
23andMe allrs797045061
SNP Nexus

SNPshotrs797045061
SNPdbers797045061
MSV3drs797045061
GWAS Ctlgrs797045061
Max Magnitude0
ClinVar
Risk rs797045061(T;T)
Alt rs797045061(T;T)
Reference Rs797045061(A;A)
Significance Pathogenic
Disease Lissencephaly 1
Variation info
Gene PAFAH1B1
CLNDBN Lissencephaly 1
Reversed 0
HGVS NC_000017.10:g.2573580A>T
CLNSRC Baylor College of Medicine
CLNACC RCV000191116.1,