rs139785364
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs139785364(A;A) |
Make rs139785364(A;G) |
Make rs139785364(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 214728759 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs139785364 |
dbSNP (classic) | rs139785364 |
ClinGen | rs139785364 |
ebi | rs139785364 |
HLI | rs139785364 |
Exac | rs139785364 |
Gnomad | rs139785364 |
Varsome | rs139785364 |
LitVar | rs139785364 |
Map | rs139785364 |
PheGenI | rs139785364 |
Biobank | rs139785364 |
1000 genomes | rs139785364 |
hgdp | rs139785364 |
ensembl | rs139785364 |
geneview | rs139785364 |
scholar | rs139785364 |
rs139785364 | |
pharmgkb | rs139785364 |
gwascentral | rs139785364 |
openSNP | rs139785364 |
23andMe | rs139785364 |
SNPshot | rs139785364 |
SNPdbe | rs139785364 |
MSV3d | rs139785364 |
GWAS Ctlg | rs139785364 |
Max Magnitude | 0 |
[PMID 23056176] Identification of Functional SNPs in BARD1 Gene and In Silico Analysis of Damaging SNPs: Based on Data Procured from dbSNP Database
ClinVar | |
---|---|
Risk | rs139785364(A;A) |
Alt | rs139785364(A;A) |
Reference | rs139785364(G;G) |
Significance | Unknown |
Disease | not specified |
Variation | info |
Gene | BARD1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.215593483G>A |
CLNSRC | |
CLNACC | RCV000484312.1, |