rs763401560
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AAGT;AAGT) | 0 | common in clinvar |
Make rs763401560(-;-) |
Make rs763401560(-;AAGT) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 152649104 |
Gene | XRCC2 |
is a | snp |
is | mentioned by |
dbSNP | rs763401560 |
dbSNP (classic) | rs763401560 |
ClinGen | rs763401560 |
ebi | rs763401560 |
HLI | rs763401560 |
Exac | rs763401560 |
Gnomad | rs763401560 |
Varsome | rs763401560 |
LitVar | rs763401560 |
Map | rs763401560 |
PheGenI | rs763401560 |
Biobank | rs763401560 |
1000 genomes | rs763401560 |
hgdp | rs763401560 |
ensembl | rs763401560 |
geneview | rs763401560 |
scholar | rs763401560 |
rs763401560 | |
pharmgkb | rs763401560 |
gwascentral | rs763401560 |
openSNP | rs763401560 |
23andMe | rs763401560 |
SNPshot | rs763401560 |
SNPdbe | rs763401560 |
MSV3d | rs763401560 |
GWAS Ctlg | rs763401560 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763401560(-;-) |
Alt | rs763401560(-;-) |
Reference | Rs763401560(AAGT;AAGT) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | XRCC2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.152346189_152346192delAAGT |
CLNSRC | |
CLNACC | RCV000481611.1, |