rs786202646
From SNPedia
Merged into | rs753153576 |
Orientation | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs786202646(A;A) |
Make rs786202646(A;C) |
Make rs786202646(C;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 23626235 |
Gene | PALB2 |
is a | snp |
is | mentioned by |
dbSNP | rs786202646 |
dbSNP (classic) | rs786202646 |
ClinGen | rs786202646 |
ebi | rs786202646 |
HLI | rs786202646 |
Exac | rs786202646 |
Gnomad | rs786202646 |
Varsome | rs786202646 |
LitVar | rs786202646 |
Map | rs786202646 |
PheGenI | rs786202646 |
Biobank | rs786202646 |
1000 genomes | rs786202646 |
hgdp | rs786202646 |
ensembl | rs786202646 |
geneview | rs786202646 |
scholar | rs786202646 |
rs786202646 | |
pharmgkb | rs786202646 |
gwascentral | rs786202646 |
openSNP | rs786202646 |
23andMe | rs786202646 |
SNPshot | rs786202646 |
SNPdbe | rs786202646 |
MSV3d | rs786202646 |
GWAS Ctlg | rs786202646 |
Status | Merged into rs753153576 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786202646(T;T) |
Alt | rs786202646(T;T) |
Reference | Rs786202646(G;G) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | PALB2 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000016.10:g.23626235C>A |
CLNSRC | |
CLNACC | RCV000165555.1, |