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rs1057517661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517661(A;A)
Make rs1057517661(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position68685628
GeneGAL, LOC107984343
is asnp
is mentioned by
dbSNPrs1057517661
dbSNP (old)rs1057517661
ClinGenrs1057517661
ebirs1057517661
HLIrs1057517661
Exacrs1057517661
Gnomadrs1057517661
Varsomers1057517661
Maprs1057517661
PheGenIrs1057517661
Biobankrs1057517661
1000 genomesrs1057517661
hgdprs1057517661
ensemblrs1057517661
gopubmedrs1057517661
geneviewrs1057517661
scholarrs1057517661
googlers1057517661
pharmgkbrs1057517661
gwascentralrs1057517661
openSNPrs1057517661
23andMers1057517661
23andMe allrs1057517661
SNPshotrs1057517661
SNPdbers1057517661
MSV3drs1057517661
GWAS Ctlgrs1057517661
Max Magnitude0
ClinVar
Risk rs1057517661(A;A)
Alt rs1057517661(A;A)
Reference Rs1057517661(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene GAL
CLNDBN Epilepsy, familial temporal lobe, 8
Reversed 0
HGVS NC_000011.9:g.68453096C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000412584.1,