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rs764276946

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs764276946(A;G)
Make rs764276946(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position68033254
GeneMIR4691, MIR7113, NDUFS8
is asnp
is mentioned by
dbSNPrs764276946
ebirs764276946
HLIrs764276946
Exacrs764276946
Varsomers764276946
Maprs764276946
PheGenIrs764276946
hapmaprs764276946
1000 genomesrs764276946
hgdprs764276946
ensemblrs764276946
gopubmedrs764276946
geneviewrs764276946
scholarrs764276946
googlers764276946
pharmgkbrs764276946
gwascentralrs764276946
openSNPrs764276946
23andMers764276946
23andMe allrs764276946
SNP Nexus

SNPshotrs764276946
SNPdbers764276946
MSV3drs764276946
GWAS Ctlgrs764276946
Max Magnitude0
ClinVar
Risk rs764276946(G;G)
Alt rs764276946(G;G)
Reference rs764276946(A;A)
Significance Probable-Pathogenic
Disease Leigh syndrome
Variation info
Gene MIR7113 MIR4691 NDUFS8
CLNDBN Leigh syndrome
Reversed 0
HGVS NC_000011.9:g.67800721A>G
CLNSRC
CLNACC RCV000200148.1,