rs121908383
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs121908383(A;G) |
Make rs121908383(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 45331502 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs121908383 |
dbSNP (classic) | rs121908383 |
ClinGen | rs121908383 |
ebi | rs121908383 |
HLI | rs121908383 |
Exac | rs121908383 |
Gnomad | rs121908383 |
Varsome | rs121908383 |
LitVar | rs121908383 |
Map | rs121908383 |
PheGenI | rs121908383 |
Biobank | rs121908383 |
1000 genomes | rs121908383 |
hgdp | rs121908383 |
ensembl | rs121908383 |
geneview | rs121908383 |
scholar | rs121908383 |
rs121908383 | |
pharmgkb | rs121908383 |
gwascentral | rs121908383 |
openSNP | rs121908383 |
23andMe | rs121908383 |
SNPshot | rs121908383 |
SNPdbe | rs121908383 |
MSV3d | rs121908383 |
GWAS Ctlg | rs121908383 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121908383(G;G) |
Alt | rs121908383(G;G) |
Reference | Rs121908383(A;A) |
Significance | Pathogenic |
Disease | Neoplasm of stomach |
Variation | info |
Gene | MUTYH |
CLNDBN | Neoplasm of stomach |
Reversed | 1 |
HGVS | NC_000001.10:g.45797174T>C |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000005620.5, |