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rs797045912

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045912(-;T)
Make rs797045912(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position103917082
GeneRELN
is asnp
is mentioned by
dbSNPrs797045912
ClinGenrs797045912
ebirs797045912
HLIrs797045912
Exacrs797045912
Varsomers797045912
Maprs797045912
PheGenIrs797045912
hapmaprs797045912
1000 genomesrs797045912
hgdprs797045912
ensemblrs797045912
gopubmedrs797045912
geneviewrs797045912
scholarrs797045912
googlers797045912
pharmgkbrs797045912
gwascentralrs797045912
openSNPrs797045912
23andMers797045912
23andMe allrs797045912
SNP Nexus

SNPshotrs797045912
SNPdbers797045912
MSV3drs797045912
GWAS Ctlgrs797045912
Max Magnitude0
ClinVar
Risk rs797045912(T;T)
Alt rs797045912(T;T)
Reference Rs797045912(-;-)
Significance Pathogenic
Disease Lissencephaly 2 (Norman-Roberts type)
Variation info
Gene RELN
CLNDBN Lissencephaly 2 (Norman-Roberts type)
Reversed 1
HGVS NC_000007.13:g.103557530dupA
CLNSRC
CLNACC RCV000192487.1,