rs796051990
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs796051990(A;G) |
Make rs796051990(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 71110040 |
Gene | MCEE |
is a | snp |
is | mentioned by |
dbSNP | rs796051990 |
dbSNP (classic) | rs796051990 |
ClinGen | rs796051990 |
ebi | rs796051990 |
HLI | rs796051990 |
Exac | rs796051990 |
Gnomad | rs796051990 |
Varsome | rs796051990 |
LitVar | rs796051990 |
Map | rs796051990 |
PheGenI | rs796051990 |
Biobank | rs796051990 |
1000 genomes | rs796051990 |
hgdp | rs796051990 |
ensembl | rs796051990 |
geneview | rs796051990 |
scholar | rs796051990 |
rs796051990 | |
pharmgkb | rs796051990 |
gwascentral | rs796051990 |
openSNP | rs796051990 |
23andMe | rs796051990 |
SNPshot | rs796051990 |
SNPdbe | rs796051990 |
MSV3d | rs796051990 |
GWAS Ctlg | rs796051990 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051990(G;G) |
Alt | rs796051990(G;G) |
Reference | Rs796051990(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MCEE |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.71337170T>C |
CLNSRC | |
CLNACC | RCV000186008.1, |