rs367838807
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs367838807(C;C) |
Make rs367838807(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 27322498 |
Gene | MPV17 |
is a | snp |
is | mentioned by |
dbSNP | rs367838807 |
dbSNP (classic) | rs367838807 |
ClinGen | rs367838807 |
ebi | rs367838807 |
HLI | rs367838807 |
Exac | rs367838807 |
Gnomad | rs367838807 |
Varsome | rs367838807 |
LitVar | rs367838807 |
Map | rs367838807 |
PheGenI | rs367838807 |
Biobank | rs367838807 |
1000 genomes | rs367838807 |
hgdp | rs367838807 |
ensembl | rs367838807 |
geneview | rs367838807 |
scholar | rs367838807 |
rs367838807 | |
pharmgkb | rs367838807 |
gwascentral | rs367838807 |
openSNP | rs367838807 |
23andMe | rs367838807 |
SNPshot | rs367838807 |
SNPdbe | rs367838807 |
MSV3d | rs367838807 |
GWAS Ctlg | rs367838807 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs367838807(C;C) |
Alt | rs367838807(C;C) |
Reference | Rs367838807(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MPV17 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.27545365T>C |
CLNSRC | |
CLNACC | RCV000199973.1, |