rs119477056
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs119477056(C;T) |
Make rs119477056(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 111585362 |
Gene | CD96 |
is a | snp |
is | mentioned by |
dbSNP | rs119477056 |
dbSNP (classic) | rs119477056 |
ClinGen | rs119477056 |
ebi | rs119477056 |
HLI | rs119477056 |
Exac | rs119477056 |
Gnomad | rs119477056 |
Varsome | rs119477056 |
LitVar | rs119477056 |
Map | rs119477056 |
PheGenI | rs119477056 |
Biobank | rs119477056 |
1000 genomes | rs119477056 |
hgdp | rs119477056 |
ensembl | rs119477056 |
geneview | rs119477056 |
scholar | rs119477056 |
rs119477056 | |
pharmgkb | rs119477056 |
gwascentral | rs119477056 |
openSNP | rs119477056 |
23andMe | rs119477056 |
SNPshot | rs119477056 |
SNPdbe | rs119477056 |
MSV3d | rs119477056 |
GWAS Ctlg | rs119477056 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs119477056(A;A) rs119477056(T;T) |
Alt | rs119477056(A;A) rs119477056(T;T) |
Reference | Rs119477056(C;C) |
Significance | Pathogenic |
Disease | C syndrome |
Variation | info |
Gene | CD96 |
CLNDBN | C syndrome |
Reversed | 0 |
HGVS | NC_000003.11:g.111304209C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000004903.2, |