rs754716792
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TC;TC) | 0 | common in clinvar |
Make rs754716792(-;-) |
Make rs754716792(-;TC) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 14 |
Position | 75046862 |
Gene | MLH3 |
is a | snp |
is | mentioned by |
dbSNP | rs754716792 |
dbSNP (classic) | rs754716792 |
ClinGen | rs754716792 |
ebi | rs754716792 |
HLI | rs754716792 |
Exac | rs754716792 |
Gnomad | rs754716792 |
Varsome | rs754716792 |
LitVar | rs754716792 |
Map | rs754716792 |
PheGenI | rs754716792 |
Biobank | rs754716792 |
1000 genomes | rs754716792 |
hgdp | rs754716792 |
ensembl | rs754716792 |
geneview | rs754716792 |
scholar | rs754716792 |
rs754716792 | |
pharmgkb | rs754716792 |
gwascentral | rs754716792 |
openSNP | rs754716792 |
23andMe | rs754716792 |
SNPshot | rs754716792 |
SNPdbe | rs754716792 |
MSV3d | rs754716792 |
GWAS Ctlg | rs754716792 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs754716792(-;-) |
Alt | rs754716792(-;-) |
Reference | Rs754716792(TC;TC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MLH3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.75513565_75513566delTC |
CLNSRC | |
CLNACC | RCV000486748.1, |