rs63750850
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6 | Lynch syndrome |
(G;G) | 0 | common in clinvar |
Make rs63750850(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 3 |
Position | 36996689 |
Gene | MLH1 |
is a | snp |
is | mentioned by |
dbSNP | rs63750850 |
dbSNP (classic) | rs63750850 |
ClinGen | rs63750850 |
ebi | rs63750850 |
HLI | rs63750850 |
Exac | rs63750850 |
Gnomad | rs63750850 |
Varsome | rs63750850 |
LitVar | rs63750850 |
Map | rs63750850 |
PheGenI | rs63750850 |
Biobank | rs63750850 |
1000 genomes | rs63750850 |
hgdp | rs63750850 |
ensembl | rs63750850 |
geneview | rs63750850 |
scholar | rs63750850 |
rs63750850 | |
pharmgkb | rs63750850 |
gwascentral | rs63750850 |
openSNP | rs63750850 |
23andMe | rs63750850 |
SNPshot | rs63750850 |
SNPdbe | rs63750850 |
MSV3d | rs63750850 |
GWAS Ctlg | rs63750850 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs63750850(A;A) |
Alt | rs63750850(A;A) |
Reference | Rs63750850(G;G) |
Significance | Probable-Pathogenic |
Disease | Lynch syndrome Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | MLH1 |
CLNDBN | Lynch syndrome Hereditary cancer-predisposing syndrome not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.37038180G>A |
CLNSRC | International Society for Gastrointestinal Hereditary Tumours |
CLNACC | RCV000075399.2, RCV000160535.5, RCV000212515.2, |