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rs780401493

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs780401493(C;T)
Make rs780401493(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position41394968
GeneNDUFAF1
is asnp
is mentioned by
dbSNPrs780401493
ebirs780401493
HLIrs780401493
Exacrs780401493
Varsomers780401493
Maprs780401493
PheGenIrs780401493
hapmaprs780401493
1000 genomesrs780401493
hgdprs780401493
ensemblrs780401493
gopubmedrs780401493
geneviewrs780401493
scholarrs780401493
googlers780401493
pharmgkbrs780401493
gwascentralrs780401493
openSNPrs780401493
23andMers780401493
23andMe allrs780401493
SNP Nexus

SNPshotrs780401493
SNPdbers780401493
MSV3drs780401493
GWAS Ctlgrs780401493
Max Magnitude0
ClinVar
Risk rs780401493(T;T)
Alt rs780401493(T;T)
Reference rs780401493(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFAF1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.41687166C>T
CLNSRC
CLNACC RCV000200677.2,