rs119486096
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs119486096(C;T) |
Make rs119486096(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 10 |
Position | 87505037 |
Gene | MINPP1 |
is a | snp |
is | mentioned by |
dbSNP | rs119486096 |
dbSNP (classic) | rs119486096 |
ClinGen | rs119486096 |
ebi | rs119486096 |
HLI | rs119486096 |
Exac | rs119486096 |
Gnomad | rs119486096 |
Varsome | rs119486096 |
LitVar | rs119486096 |
Map | rs119486096 |
PheGenI | rs119486096 |
Biobank | rs119486096 |
1000 genomes | rs119486096 |
hgdp | rs119486096 |
ensembl | rs119486096 |
geneview | rs119486096 |
scholar | rs119486096 |
rs119486096 | |
pharmgkb | rs119486096 |
gwascentral | rs119486096 |
openSNP | rs119486096 |
23andMe | rs119486096 |
SNPshot | rs119486096 |
SNPdbe | rs119486096 |
MSV3d | rs119486096 |
GWAS Ctlg | rs119486096 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs119486096(T;T) |
Alt | rs119486096(T;T) |
Reference | Rs119486096(C;C) |
Significance | Pathogenic |
Disease | Thyroid cancer |
Variation | info |
Gene | MINPP1 |
CLNDBN | Thyroid cancer, follicular |
Reversed | 0 |
HGVS | NC_000010.10:g.89264794C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000005324.4, |