rs863223932
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(D;D) | 0 | common genotype |
Make rs863223932(-;TGCTCCCTGC) |
Make rs863223932(TGCTCCCTGC;TGCTCCCTGC) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 8 |
Position | 95032039 |
Gene | NDUFAF6 |
is a | snp |
is | mentioned by |
dbSNP | rs863223932 |
dbSNP (classic) | rs863223932 |
ClinGen | rs863223932 |
ebi | rs863223932 |
HLI | rs863223932 |
Exac | rs863223932 |
Gnomad | rs863223932 |
Varsome | rs863223932 |
LitVar | rs863223932 |
Map | rs863223932 |
PheGenI | rs863223932 |
Biobank | rs863223932 |
1000 genomes | rs863223932 |
hgdp | rs863223932 |
ensembl | rs863223932 |
geneview | rs863223932 |
scholar | rs863223932 |
rs863223932 | |
pharmgkb | rs863223932 |
gwascentral | rs863223932 |
openSNP | rs863223932 |
23andMe | rs863223932 |
SNPshot | rs863223932 |
SNPdbe | rs863223932 |
MSV3d | rs863223932 |
GWAS Ctlg | rs863223932 |
Max Magnitude | 0 |
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, |