rs879254317
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs879254317(G;T) |
Make rs879254317(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 5 |
Position | 149027244 |
Gene | SH3TC2 |
is a | snp |
is | mentioned by |
dbSNP | rs879254317 |
dbSNP (classic) | rs879254317 |
ClinGen | rs879254317 |
ebi | rs879254317 |
HLI | rs879254317 |
Exac | rs879254317 |
Gnomad | rs879254317 |
Varsome | rs879254317 |
LitVar | rs879254317 |
Map | rs879254317 |
PheGenI | rs879254317 |
Biobank | rs879254317 |
1000 genomes | rs879254317 |
hgdp | rs879254317 |
ensembl | rs879254317 |
geneview | rs879254317 |
scholar | rs879254317 |
rs879254317 | |
pharmgkb | rs879254317 |
gwascentral | rs879254317 |
openSNP | rs879254317 |
23andMe | rs879254317 |
SNPshot | rs879254317 |
SNPdbe | rs879254317 |
MSV3d | rs879254317 |
GWAS Ctlg | rs879254317 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879254317(T;T) |
Alt | rs879254317(T;T) |
Reference | Rs879254317(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SH3TC2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000005.9:g.148406807C>A |
CLNSRC | |
CLNACC | RCV000235715.1, |