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rs201044262

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201044262(A;A)
Make rs201044262(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position103640597
GeneRELN
is asnp
is mentioned by
dbSNPrs201044262
ebirs201044262
HLIrs201044262
Exacrs201044262
Varsomers201044262
Maprs201044262
PheGenIrs201044262
hapmaprs201044262
1000 genomesrs201044262
hgdprs201044262
ensemblrs201044262
gopubmedrs201044262
geneviewrs201044262
scholarrs201044262
googlers201044262
pharmgkbrs201044262
gwascentralrs201044262
openSNPrs201044262
23andMers201044262
23andMe allrs201044262
SNP Nexus

SNPshotrs201044262
SNPdbers201044262
MSV3drs201044262
GWAS Ctlgrs201044262
Max Magnitude0
ClinVar
Risk rs201044262(A;A)
Alt rs201044262(A;A)
Reference rs201044262(G;G)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene RELN
CLNDBN Epilepsy, familial temporal lobe, 7
Reversed 0
HGVS NC_000007.13:g.103281044G>A
CLNSRC
CLNACC RCV000193679.1,