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rs863223932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223932(-;TGCTCCCTGC)
Make rs863223932(TGCTCCCTGC;TGCTCCCTGC)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position95032039
GeneNDUFAF6
is asnp
is mentioned by
dbSNPrs863223932
dbSNP (old)rs863223932
ClinGenrs863223932
ebirs863223932
HLIrs863223932
Exacrs863223932
Varsomers863223932
Maprs863223932
PheGenIrs863223932
Biobankrs863223932
1000 genomesrs863223932
hgdprs863223932
ensemblrs863223932
gopubmedrs863223932
geneviewrs863223932
scholarrs863223932
googlers863223932
pharmgkbrs863223932
gwascentralrs863223932
openSNPrs863223932
23andMers863223932
23andMe allrs863223932
SNP Nexus

SNPshotrs863223932
SNPdbers863223932
MSV3drs863223932
GWAS Ctlgrs863223932
Max Magnitude0
ClinVar
Risk rs863223932(TGCTCCCTGC;TGCTCCCTGC)
Alt rs863223932(TGCTCCCTGC;TGCTCCCTGC)
Reference Rs863223932(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFAF6
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.96044258_96044267dupTGCTCCCTGC
CLNSRC
CLNACC RCV000200694.1,