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rs863223931

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs863223931(-;-)
Make rs863223931(-;TC)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position95035463
GeneNDUFAF6
is asnp
is mentioned by
dbSNPrs863223931
dbSNP (old)rs863223931
ClinGenrs863223931
ebirs863223931
HLIrs863223931
Exacrs863223931
Gnomadrs863223931
Varsomers863223931
Maprs863223931
PheGenIrs863223931
Biobankrs863223931
1000 genomesrs863223931
hgdprs863223931
ensemblrs863223931
gopubmedrs863223931
geneviewrs863223931
scholarrs863223931
googlers863223931
pharmgkbrs863223931
gwascentralrs863223931
openSNPrs863223931
23andMers863223931
23andMe allrs863223931
SNP Nexus

SNPshotrs863223931
SNPdbers863223931
MSV3drs863223931
GWAS Ctlgrs863223931
Max Magnitude0
ClinVar
Risk rs863223931(-;-) Rs863223931(CT;CT)
Alt rs863223931(-;-) Rs863223931(CT;CT)
Reference Rs863223931(TC;TC)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFAF6
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.96047691_96047692delTC
CLNSRC
CLNACC RCV000196917.1,