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rs797044997

From SNPedia

Orientationplus
Make rs797044997(-;-)
Make rs797044997(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93793270
GeneLGI1
is asnp
is mentioned by
dbSNPrs797044997
ebirs797044997
HLIrs797044997
Exacrs797044997
Varsomers797044997
Maprs797044997
PheGenIrs797044997
hapmaprs797044997
1000 genomesrs797044997
hgdprs797044997
ensemblrs797044997
gopubmedrs797044997
geneviewrs797044997
scholarrs797044997
googlers797044997
pharmgkbrs797044997
gwascentralrs797044997
openSNPrs797044997
23andMers797044997
23andMe allrs797044997
SNP Nexus

SNPshotrs797044997
SNPdbers797044997
MSV3drs797044997
GWAS Ctlgrs797044997
Max Magnitude
ClinVar
Risk rs797044997(;)
Alt rs797044997(;)
Reference rs797044997(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene LGI1
CLNDBN Epilepsy, lateral temporal lobe, autosomal dominant
Reversed 0
HGVS NC_000010.10:g.95553027delC
CLNSRC
CLNACC RCV000195148.1,