rs765835040
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs765835040(C;T) |
Make rs765835040(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 44857158 |
Gene | EFTUD2 |
is a | snp |
is | mentioned by |
dbSNP | rs765835040 |
dbSNP (classic) | rs765835040 |
ClinGen | rs765835040 |
ebi | rs765835040 |
HLI | rs765835040 |
Exac | rs765835040 |
Gnomad | rs765835040 |
Varsome | rs765835040 |
LitVar | rs765835040 |
Map | rs765835040 |
PheGenI | rs765835040 |
Biobank | rs765835040 |
1000 genomes | rs765835040 |
hgdp | rs765835040 |
ensembl | rs765835040 |
geneview | rs765835040 |
scholar | rs765835040 |
rs765835040 | |
pharmgkb | rs765835040 |
gwascentral | rs765835040 |
openSNP | rs765835040 |
23andMe | rs765835040 |
SNPshot | rs765835040 |
SNPdbe | rs765835040 |
MSV3d | rs765835040 |
GWAS Ctlg | rs765835040 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs765835040(A;A) rs765835040(T;T) |
Alt | rs765835040(A;A) rs765835040(T;T) |
Reference | Rs765835040(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | EFTUD2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.42934526C>A |
CLNSRC | |
CLNACC | RCV000479806.1, |