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rs754843709

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754843709(A;A)
Make rs754843709(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position68036361
GeneNDUFS8
is asnp
is mentioned by
dbSNPrs754843709
ebirs754843709
HLIrs754843709
Exacrs754843709
Varsomers754843709
Maprs754843709
PheGenIrs754843709
hapmaprs754843709
1000 genomesrs754843709
hgdprs754843709
ensemblrs754843709
gopubmedrs754843709
geneviewrs754843709
scholarrs754843709
googlers754843709
pharmgkbrs754843709
gwascentralrs754843709
openSNPrs754843709
23andMers754843709
23andMe allrs754843709
SNP Nexus

SNPshotrs754843709
SNPdbers754843709
MSV3drs754843709
GWAS Ctlgrs754843709
Max Magnitude0
ClinVar
Risk rs754843709(A;A)
Alt rs754843709(A;A)
Reference rs754843709(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS8
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67803828C>A
CLNSRC
CLNACC RCV000196020.1,