rs786205634
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs786205634(-;-) |
Make rs786205634(-;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 85663648 |
Gene | SFTPB |
is a | snp |
is | mentioned by |
dbSNP | rs786205634 |
dbSNP (classic) | rs786205634 |
ClinGen | rs786205634 |
ebi | rs786205634 |
HLI | rs786205634 |
Exac | rs786205634 |
Gnomad | rs786205634 |
Varsome | rs786205634 |
LitVar | rs786205634 |
Map | rs786205634 |
PheGenI | rs786205634 |
Biobank | rs786205634 |
1000 genomes | rs786205634 |
hgdp | rs786205634 |
ensembl | rs786205634 |
geneview | rs786205634 |
scholar | rs786205634 |
rs786205634 | |
pharmgkb | rs786205634 |
gwascentral | rs786205634 |
openSNP | rs786205634 |
23andMe | rs786205634 |
SNPshot | rs786205634 |
SNPdbe | rs786205634 |
MSV3d | rs786205634 |
GWAS Ctlg | rs786205634 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205634(-;-) |
Alt | rs786205634(-;-) |
Reference | Rs786205634(A;A) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | SFTPB |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000002.11:g.85890771delT |
CLNSRC | |
CLNACC | RCV000171496.2, |