rs794728688
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs794728688(A;A) |
Make rs794728688(A;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 43123808 |
Gene | RET |
is a | snp |
is | mentioned by |
dbSNP | rs794728688 |
dbSNP (classic) | rs794728688 |
ClinGen | rs794728688 |
ebi | rs794728688 |
HLI | rs794728688 |
Exac | rs794728688 |
Gnomad | rs794728688 |
Varsome | rs794728688 |
LitVar | rs794728688 |
Map | rs794728688 |
PheGenI | rs794728688 |
Biobank | rs794728688 |
1000 genomes | rs794728688 |
hgdp | rs794728688 |
ensembl | rs794728688 |
geneview | rs794728688 |
scholar | rs794728688 |
rs794728688 | |
pharmgkb | rs794728688 |
gwascentral | rs794728688 |
openSNP | rs794728688 |
23andMe | rs794728688 |
SNPshot | rs794728688 |
SNPdbe | rs794728688 |
MSV3d | rs794728688 |
GWAS Ctlg | rs794728688 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794728688(A;A) |
Alt | rs794728688(A;A) |
Reference | Rs794728688(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | RET |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.43619256T>A |
CLNSRC | |
CLNACC | RCV000182589.1, |