rs63750722
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;AGGA) | 6 | Lynch syndrome, pathogenic mutation |
(AAGG;AAGG) | 0 | common in clinvar |
(AGGA;AGGA) | 0 | common in clinvar |
(D;D) | 0 |
Make rs63750722(-;-) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 47476521 |
Gene | MSH2 |
is a | snp |
is | mentioned by |
dbSNP | rs63750722 |
dbSNP (classic) | rs63750722 |
ClinGen | rs63750722 |
ebi | rs63750722 |
HLI | rs63750722 |
Exac | rs63750722 |
Gnomad | rs63750722 |
Varsome | rs63750722 |
LitVar | rs63750722 |
Map | rs63750722 |
PheGenI | rs63750722 |
Biobank | rs63750722 |
1000 genomes | rs63750722 |
hgdp | rs63750722 |
ensembl | rs63750722 |
geneview | rs63750722 |
scholar | rs63750722 |
rs63750722 | |
pharmgkb | rs63750722 |
gwascentral | rs63750722 |
openSNP | rs63750722 |
23andMe | rs63750722 |
SNPshot | rs63750722 |
SNPdbe | rs63750722 |
MSV3d | rs63750722 |
GWAS Ctlg | rs63750722 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs63750722(-;-) |
Alt | rs63750722(-;-) |
Reference | Rs63750722(AAGG;AAGG) |
Significance | Pathogenic |
Disease | Lynch syndrome |
Variation | info |
Gene | MSH2 |
CLNDBN | Lynch syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.47703660_47703663delAGGA |
CLNSRC | International Society for Gastrointestinal Hereditary Tumours |
CLNACC | RCV000076413.2, |