rs863224194
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs863224194(A;G) |
Make rs863224194(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 8 |
Position | 102226036 |
Gene | RRM2B |
is a | snp |
is | mentioned by |
dbSNP | rs863224194 |
dbSNP (classic) | rs863224194 |
ClinGen | rs863224194 |
ebi | rs863224194 |
HLI | rs863224194 |
Exac | rs863224194 |
Gnomad | rs863224194 |
Varsome | rs863224194 |
LitVar | rs863224194 |
Map | rs863224194 |
PheGenI | rs863224194 |
Biobank | rs863224194 |
1000 genomes | rs863224194 |
hgdp | rs863224194 |
ensembl | rs863224194 |
geneview | rs863224194 |
scholar | rs863224194 |
rs863224194 | |
pharmgkb | rs863224194 |
gwascentral | rs863224194 |
openSNP | rs863224194 |
23andMe | rs863224194 |
SNPshot | rs863224194 |
SNPdbe | rs863224194 |
MSV3d | rs863224194 |
GWAS Ctlg | rs863224194 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224194(G;G) |
Alt | rs863224194(G;G) |
Reference | Rs863224194(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | RRM2B |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000008.10:g.103238264T>C |
CLNSRC | |
CLNACC | RCV000200520.2, |