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rs869320767

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320767(A;A)
Make rs869320767(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position103553659
GeneRELN
is asnp
is mentioned by
dbSNPrs869320767
ebirs869320767
HLIrs869320767
Exacrs869320767
Varsomers869320767
Maprs869320767
PheGenIrs869320767
hapmaprs869320767
1000 genomesrs869320767
hgdprs869320767
ensemblrs869320767
gopubmedrs869320767
geneviewrs869320767
scholarrs869320767
googlers869320767
pharmgkbrs869320767
gwascentralrs869320767
openSNPrs869320767
23andMers869320767
23andMe allrs869320767
SNP Nexus

SNPshotrs869320767
SNPdbers869320767
MSV3drs869320767
GWAS Ctlgrs869320767
Max Magnitude0
ClinVar
Risk rs869320767(A;A)
Alt rs869320767(A;A)
Reference rs869320767(G;G)
Significance Pathogenic
Disease Lissencephaly 2
Variation info
Gene RELN
CLNDBN Lissencephaly 2
Reversed 1
HGVS NC_000007.13:g.103194106C>T
CLNSRC
CLNACC RCV000210930.1,