rs267607744
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;G) | 6 | Lynch syndrome |
(G;G) | 0 | common in clinvar |
Make rs267607744(A;A) |
Make rs267607744(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 37006990 |
Gene | MLH1 |
is a | snp |
is | mentioned by |
dbSNP | rs267607744 |
dbSNP (classic) | rs267607744 |
ClinGen | rs267607744 |
ebi | rs267607744 |
HLI | rs267607744 |
Exac | rs267607744 |
Gnomad | rs267607744 |
Varsome | rs267607744 |
LitVar | rs267607744 |
Map | rs267607744 |
PheGenI | rs267607744 |
Biobank | rs267607744 |
1000 genomes | rs267607744 |
hgdp | rs267607744 |
ensembl | rs267607744 |
geneview | rs267607744 |
scholar | rs267607744 |
rs267607744 | |
pharmgkb | rs267607744 |
gwascentral | rs267607744 |
openSNP | rs267607744 |
23andMe | rs267607744 |
SNPshot | rs267607744 |
SNPdbe | rs267607744 |
MSV3d | rs267607744 |
GWAS Ctlg | rs267607744 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs267607744(A;A) |
Alt | rs267607744(A;A) |
Reference | Rs267607744(G;G) |
Significance | Pathogenic |
Disease | Lynch syndrome not provided |
Variation | info |
Gene | MLH1 |
CLNDBN | Lynch syndrome not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.37048481G>A |
CLNSRC | |
CLNACC | RCV000205947.3, RCV000480828.1, |