rs148317871
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs148317871(A;A) |
Make rs148317871(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 37050595 |
Gene | MLH1 |
is a | snp |
is | mentioned by |
dbSNP | rs148317871 |
dbSNP (classic) | rs148317871 |
ClinGen | rs148317871 |
ebi | rs148317871 |
HLI | rs148317871 |
Exac | rs148317871 |
Gnomad | rs148317871 |
Varsome | rs148317871 |
LitVar | rs148317871 |
Map | rs148317871 |
PheGenI | rs148317871 |
Biobank | rs148317871 |
1000 genomes | rs148317871 |
hgdp | rs148317871 |
ensembl | rs148317871 |
geneview | rs148317871 |
scholar | rs148317871 |
rs148317871 | |
pharmgkb | rs148317871 |
gwascentral | rs148317871 |
openSNP | rs148317871 |
23andMe | rs148317871 |
SNPshot | rs148317871 |
SNPdbe | rs148317871 |
MSV3d | rs148317871 |
GWAS Ctlg | rs148317871 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs148317871(A;A) |
Alt | rs148317871(A;A) |
Reference | Rs148317871(G;G) |
Significance | Other |
Disease | Lynch syndrome not specified Lynch syndrome II |
Variation | info |
Gene | MLH1 |
CLNDBN | Lynch syndrome not specified Lynch syndrome II |
Reversed | 0 |
HGVS | NC_000003.11:g.37092086G>A |
CLNSRC | ClinVar LabCorp |
CLNACC | RCV000030221.3, RCV000160545.3, RCV000411992.1, |