rs754367349
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs754367349(-;-) |
Make rs754367349(-;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 58709927 |
Gene | RAD51C |
is a | snp |
is | mentioned by |
dbSNP | rs754367349 |
dbSNP (classic) | rs754367349 |
ClinGen | rs754367349 |
ebi | rs754367349 |
HLI | rs754367349 |
Exac | rs754367349 |
Gnomad | rs754367349 |
Varsome | rs754367349 |
LitVar | rs754367349 |
Map | rs754367349 |
PheGenI | rs754367349 |
Biobank | rs754367349 |
1000 genomes | rs754367349 |
hgdp | rs754367349 |
ensembl | rs754367349 |
geneview | rs754367349 |
scholar | rs754367349 |
rs754367349 | |
pharmgkb | rs754367349 |
gwascentral | rs754367349 |
openSNP | rs754367349 |
23andMe | rs754367349 |
SNPshot | rs754367349 |
SNPdbe | rs754367349 |
MSV3d | rs754367349 |
GWAS Ctlg | rs754367349 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs754367349(-;-) |
Alt | rs754367349(-;-) |
Reference | Rs754367349(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | RAD51C |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.56787288delT |
CLNSRC | |
CLNACC | RCV000484016.1, |