rs377153250
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs377153250(C;C) |
Make rs377153250(C;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 214780658 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs377153250 |
dbSNP (classic) | rs377153250 |
ClinGen | rs377153250 |
ebi | rs377153250 |
HLI | rs377153250 |
Exac | rs377153250 |
Gnomad | rs377153250 |
Varsome | rs377153250 |
LitVar | rs377153250 |
Map | rs377153250 |
PheGenI | rs377153250 |
Biobank | rs377153250 |
1000 genomes | rs377153250 |
hgdp | rs377153250 |
ensembl | rs377153250 |
geneview | rs377153250 |
scholar | rs377153250 |
rs377153250 | |
pharmgkb | rs377153250 |
gwascentral | rs377153250 |
openSNP | rs377153250 |
23andMe | rs377153250 |
SNPshot | rs377153250 |
SNPdbe | rs377153250 |
MSV3d | rs377153250 |
GWAS Ctlg | rs377153250 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs377153250(A;A) rs377153250(C;C) |
Alt | rs377153250(A;A) rs377153250(C;C) |
Reference | Rs377153250(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not specified |
Variation | info |
Gene | BARD1 |
CLNDBN | Hereditary cancer-predisposing syndrome not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.215645382G>A; NC_000002.11:g.215645382G>C |
CLNSRC | |
CLNACC | RCV000217217.1, RCV000130569.5, RCV000212125.1, |