rs34960210
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(T;T) | 0 | common in clinvar |
Make rs34960210(-;A) |
Make rs34960210(A;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 8 |
Position | 95035578 |
Gene | NDUFAF6 |
is a | snp |
is | mentioned by |
dbSNP | rs34960210 |
dbSNP (classic) | rs34960210 |
ClinGen | rs34960210 |
ebi | rs34960210 |
HLI | rs34960210 |
Exac | rs34960210 |
Gnomad | rs34960210 |
Varsome | rs34960210 |
LitVar | rs34960210 |
Map | rs34960210 |
PheGenI | rs34960210 |
Biobank | rs34960210 |
1000 genomes | rs34960210 |
hgdp | rs34960210 |
ensembl | rs34960210 |
geneview | rs34960210 |
scholar | rs34960210 |
rs34960210 | |
pharmgkb | rs34960210 |
gwascentral | rs34960210 |
openSNP | rs34960210 |
23andMe | rs34960210 |
SNPshot | rs34960210 |
SNPdbe | rs34960210 |
MSV3d | rs34960210 |
GWAS Ctlg | rs34960210 |
Max Magnitude | 0 |
aka c.420+2dup
ClinVar | |
---|---|
Risk | rs34960210(A;A) rs34960210(AA;AA) rs34960210(AAA;AAA) rs34960210(AAAA;AAAA) Rs34960210(T;T) |
Alt | rs34960210(A;A) rs34960210(AA;AA) rs34960210(AAA;AAA) rs34960210(AAAA;AAAA) Rs34960210(T;T) |
Reference | Rs34960210(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | NDUFAF6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000008.10:g.96047806dupT |
CLNSRC | |
CLNACC | RCV000198813.1, |