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rs768892194

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs768892194(C;C)
Make rs768892194(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position61073208
GeneNDUFAF2
is asnp
is mentioned by
dbSNPrs768892194
ebirs768892194
HLIrs768892194
Exacrs768892194
Varsomers768892194
Maprs768892194
PheGenIrs768892194
hapmaprs768892194
1000 genomesrs768892194
hgdprs768892194
ensemblrs768892194
gopubmedrs768892194
geneviewrs768892194
scholarrs768892194
googlers768892194
pharmgkbrs768892194
gwascentralrs768892194
openSNPrs768892194
23andMers768892194
23andMe allrs768892194
SNP Nexus

SNPshotrs768892194
SNPdbers768892194
MSV3drs768892194
GWAS Ctlgrs768892194
Max Magnitude0
ClinVar
Risk rs768892194(C;C)
Alt rs768892194(C;C)
Reference rs768892194(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFAF2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.60369035T>C
CLNSRC
CLNACC RCV000196143.1,