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rs587780435

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780435(A;A)
Make rs587780435(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position103565295
GeneRELN
is asnp
is mentioned by
dbSNPrs587780435
ebirs587780435
HLIrs587780435
Exacrs587780435
Varsomers587780435
Maprs587780435
PheGenIrs587780435
hapmaprs587780435
1000 genomesrs587780435
hgdprs587780435
ensemblrs587780435
gopubmedrs587780435
geneviewrs587780435
scholarrs587780435
googlers587780435
pharmgkbrs587780435
gwascentralrs587780435
openSNPrs587780435
23andMers587780435
23andMe allrs587780435
SNP Nexus

SNPshotrs587780435
SNPdbers587780435
MSV3drs587780435
GWAS Ctlgrs587780435
Max Magnitude0
ClinVar
Risk rs587780435(A;A)
Alt rs587780435(A;A)
Reference rs587780435(C;C)
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.103205742G>T
CLNSRC
CLNACC RCV000118138.1,