rs375681722
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs375681722(C;T) |
Make rs375681722(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 78702289 |
Gene | TENM4 |
is a | snp |
is | mentioned by |
dbSNP | rs375681722 |
dbSNP (classic) | rs375681722 |
ClinGen | rs375681722 |
ebi | rs375681722 |
HLI | rs375681722 |
Exac | rs375681722 |
Gnomad | rs375681722 |
Varsome | rs375681722 |
LitVar | rs375681722 |
Map | rs375681722 |
PheGenI | rs375681722 |
Biobank | rs375681722 |
1000 genomes | rs375681722 |
hgdp | rs375681722 |
ensembl | rs375681722 |
geneview | rs375681722 |
scholar | rs375681722 |
rs375681722 | |
pharmgkb | rs375681722 |
gwascentral | rs375681722 |
openSNP | rs375681722 |
23andMe | rs375681722 |
SNPshot | rs375681722 |
SNPdbe | rs375681722 |
MSV3d | rs375681722 |
GWAS Ctlg | rs375681722 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs375681722(T;T) |
Alt | rs375681722(T;T) |
Reference | Rs375681722(C;C) |
Significance | Pathogenic |
Disease | Tremor |
Variation | info |
Gene | TENM4 |
CLNDBN | Tremor, hereditary essential, 5 |
Reversed | 0 |
HGVS | NC_000011.9:g.78413334C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000203527.1, |