rs749466673
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs749466673(A;A) |
Make rs749466673(A;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 132595041 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs749466673 |
dbSNP (classic) | rs749466673 |
ClinGen | rs749466673 |
ebi | rs749466673 |
HLI | rs749466673 |
Exac | rs749466673 |
Gnomad | rs749466673 |
Varsome | rs749466673 |
LitVar | rs749466673 |
Map | rs749466673 |
PheGenI | rs749466673 |
Biobank | rs749466673 |
1000 genomes | rs749466673 |
hgdp | rs749466673 |
ensembl | rs749466673 |
geneview | rs749466673 |
scholar | rs749466673 |
rs749466673 | |
pharmgkb | rs749466673 |
gwascentral | rs749466673 |
openSNP | rs749466673 |
23andMe | rs749466673 |
SNPshot | rs749466673 |
SNPdbe | rs749466673 |
MSV3d | rs749466673 |
GWAS Ctlg | rs749466673 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs749466673(A;A) rs749466673(T;T) |
Alt | rs749466673(A;A) rs749466673(T;T) |
Reference | Rs749466673(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131930733C>T |
CLNSRC | |
CLNACC | RCV000229634.1, |