rs756981921
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs756981921(A;C) |
Make rs756981921(C;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 193642808 |
Gene | OPA1 |
is a | snp |
is | mentioned by |
dbSNP | rs756981921 |
dbSNP (classic) | rs756981921 |
ClinGen | rs756981921 |
ebi | rs756981921 |
HLI | rs756981921 |
Exac | rs756981921 |
Gnomad | rs756981921 |
Varsome | rs756981921 |
LitVar | rs756981921 |
Map | rs756981921 |
PheGenI | rs756981921 |
Biobank | rs756981921 |
1000 genomes | rs756981921 |
hgdp | rs756981921 |
ensembl | rs756981921 |
geneview | rs756981921 |
scholar | rs756981921 |
rs756981921 | |
pharmgkb | rs756981921 |
gwascentral | rs756981921 |
openSNP | rs756981921 |
23andMe | rs756981921 |
SNPshot | rs756981921 |
SNPdbe | rs756981921 |
MSV3d | rs756981921 |
GWAS Ctlg | rs756981921 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs756981921(C;C) |
Alt | rs756981921(C;C) |
Reference | Rs756981921(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | OPA1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.193360597A>C |
CLNSRC | |
CLNACC | RCV000197106.1, |