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rs794726964

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726964(G;T)
Make rs794726964(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position18121943
GeneNHLRC1
is asnp
is mentioned by
dbSNPrs794726964
ebirs794726964
HLIrs794726964
Exacrs794726964
Varsomers794726964
Maprs794726964
PheGenIrs794726964
hapmaprs794726964
1000 genomesrs794726964
hgdprs794726964
ensemblrs794726964
gopubmedrs794726964
geneviewrs794726964
scholarrs794726964
googlers794726964
pharmgkbrs794726964
gwascentralrs794726964
openSNPrs794726964
23andMers794726964
23andMe allrs794726964
SNP Nexus

SNPshotrs794726964
SNPdbers794726964
MSV3drs794726964
GWAS Ctlgrs794726964
Max Magnitude0
ClinVar
Risk rs794726964(T;T)
Alt rs794726964(T;T)
Reference rs794726964(G;G)
Significance Pathogenic
Disease Lafora disease
Variation info
Gene NHLRC1
CLNDBN Lafora disease
Reversed 1
HGVS NC_000006.11:g.18122174C>A
CLNSRC
CLNACC RCV000173592.1,