Have questions? Visit https://www.reddit.com/r/SNPedia

rs587780437

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780437(A;A)
Make rs587780437(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position103523390
GeneRELN
is asnp
is mentioned by
dbSNPrs587780437
ebirs587780437
HLIrs587780437
Exacrs587780437
Varsomers587780437
Maprs587780437
PheGenIrs587780437
hapmaprs587780437
1000 genomesrs587780437
hgdprs587780437
ensemblrs587780437
gopubmedrs587780437
geneviewrs587780437
scholarrs587780437
googlers587780437
pharmgkbrs587780437
gwascentralrs587780437
openSNPrs587780437
23andMers587780437
23andMe allrs587780437
SNP Nexus

SNPshotrs587780437
SNPdbers587780437
MSV3drs587780437
GWAS Ctlgrs587780437
Max Magnitude0
ClinVar
Risk rs587780437(A;A)
Alt rs587780437(A;A)
Reference rs587780437(G;G)
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.103163837C>T
CLNSRC
CLNACC RCV000118140.1,