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rs768119894

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs768119894(C;C)
Make rs768119894(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position103636370
GeneRELN
is asnp
is mentioned by
dbSNPrs768119894
ebirs768119894
HLIrs768119894
Exacrs768119894
Varsomers768119894
Maprs768119894
PheGenIrs768119894
hapmaprs768119894
1000 genomesrs768119894
hgdprs768119894
ensemblrs768119894
gopubmedrs768119894
geneviewrs768119894
scholarrs768119894
googlers768119894
pharmgkbrs768119894
gwascentralrs768119894
openSNPrs768119894
23andMers768119894
23andMe allrs768119894
SNP Nexus

SNPshotrs768119894
SNPdbers768119894
MSV3drs768119894
GWAS Ctlgrs768119894
Max Magnitude0
ClinVar
Risk rs768119894(C;C)
Alt rs768119894(C;C)
Reference rs768119894(T;T)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene RELN
CLNDBN Epilepsy, familial temporal lobe, 7
Reversed 0
HGVS NC_000007.13:g.103276817T>C
CLNSRC
CLNACC RCV000194189.1,