rs397517059
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs397517059(C;T) |
Make rs397517059(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 34793389 |
Gene | ACTC1, LOC101928174 |
is a | snp |
is | mentioned by |
dbSNP | rs397517059 |
dbSNP (classic) | rs397517059 |
ClinGen | rs397517059 |
ebi | rs397517059 |
HLI | rs397517059 |
Exac | rs397517059 |
Gnomad | rs397517059 |
Varsome | rs397517059 |
LitVar | rs397517059 |
Map | rs397517059 |
PheGenI | rs397517059 |
Biobank | rs397517059 |
1000 genomes | rs397517059 |
hgdp | rs397517059 |
ensembl | rs397517059 |
geneview | rs397517059 |
scholar | rs397517059 |
rs397517059 | |
pharmgkb | rs397517059 |
gwascentral | rs397517059 |
openSNP | rs397517059 |
23andMe | rs397517059 |
SNPshot | rs397517059 |
SNPdbe | rs397517059 |
MSV3d | rs397517059 |
GWAS Ctlg | rs397517059 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397517059(T;T) |
Alt | rs397517059(T;T) |
Reference | Rs397517059(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | ACTC1 LOC101928174 RP11-814P5.1 |
CLNDBN | not specified not provided |
Reversed | 1 |
HGVS | NC_000015.9:g.35085590G>A |
CLNSRC | |
CLNACC | RCV000038325.3, RCV000484679.1, |