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rs769301934

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769301934(C;T)
Make rs769301934(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position18122171
GeneNHLRC1
is asnp
is mentioned by
dbSNPrs769301934
ebirs769301934
HLIrs769301934
Exacrs769301934
Varsomers769301934
Maprs769301934
PheGenIrs769301934
hapmaprs769301934
1000 genomesrs769301934
hgdprs769301934
ensemblrs769301934
gopubmedrs769301934
geneviewrs769301934
scholarrs769301934
googlers769301934
pharmgkbrs769301934
gwascentralrs769301934
openSNPrs769301934
23andMers769301934
23andMe allrs769301934
SNP Nexus

SNPshotrs769301934
SNPdbers769301934
MSV3drs769301934
GWAS Ctlgrs769301934
Max Magnitude0
ClinVar
Risk rs769301934(T;T)
Alt rs769301934(T;T)
Reference rs769301934(C;C)
Significance Pathogenic
Disease not provided Lafora disease
Variation info
Gene NHLRC1
CLNDBN not provided Lafora disease
Reversed 0
HGVS NC_000006.11:g.18122402C>T
CLNSRC
CLNACC RCV000188209.1, RCV000192027.1,