rs560785131
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs560785131(C;T) |
Make rs560785131(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 152676040 |
Gene | XRCC2 |
is a | snp |
is | mentioned by |
dbSNP | rs560785131 |
dbSNP (classic) | rs560785131 |
ClinGen | rs560785131 |
ebi | rs560785131 |
HLI | rs560785131 |
Exac | rs560785131 |
Gnomad | rs560785131 |
Varsome | rs560785131 |
LitVar | rs560785131 |
Map | rs560785131 |
PheGenI | rs560785131 |
Biobank | rs560785131 |
1000 genomes | rs560785131 |
hgdp | rs560785131 |
ensembl | rs560785131 |
geneview | rs560785131 |
scholar | rs560785131 |
rs560785131 | |
pharmgkb | rs560785131 |
gwascentral | rs560785131 |
openSNP | rs560785131 |
23andMe | rs560785131 |
SNPshot | rs560785131 |
SNPdbe | rs560785131 |
MSV3d | rs560785131 |
GWAS Ctlg | rs560785131 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs560785131(T;T) |
Alt | rs560785131(T;T) |
Reference | Rs560785131(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | XRCC2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.152373125C>T |
CLNSRC | |
CLNACC | RCV000484345.1, |