rs777937955
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs777937955(G;T) |
Make rs777937955(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 214752502 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs777937955 |
dbSNP (classic) | rs777937955 |
ClinGen | rs777937955 |
ebi | rs777937955 |
HLI | rs777937955 |
Exac | rs777937955 |
Gnomad | rs777937955 |
Varsome | rs777937955 |
LitVar | rs777937955 |
Map | rs777937955 |
PheGenI | rs777937955 |
Biobank | rs777937955 |
1000 genomes | rs777937955 |
hgdp | rs777937955 |
ensembl | rs777937955 |
geneview | rs777937955 |
scholar | rs777937955 |
rs777937955 | |
pharmgkb | rs777937955 |
gwascentral | rs777937955 |
openSNP | rs777937955 |
23andMe | rs777937955 |
SNPshot | rs777937955 |
SNPdbe | rs777937955 |
MSV3d | rs777937955 |
GWAS Ctlg | rs777937955 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs777937955(A;A) rs777937955(T;T) |
Alt | rs777937955(A;A) rs777937955(T;T) |
Reference | Rs777937955(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | BARD1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.215617226G>T |
CLNSRC | |
CLNACC | RCV000438118.1, |