rs387906389
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GATGA;GATGA) | 0 | common in clinvar |
Make rs387906389(-;-) |
Make rs387906389(-;GATGA) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 51986840 |
Gene | ACVR1B |
is a | snp |
is | mentioned by |
dbSNP | rs387906389 |
dbSNP (classic) | rs387906389 |
ClinGen | rs387906389 |
ebi | rs387906389 |
HLI | rs387906389 |
Exac | rs387906389 |
Gnomad | rs387906389 |
Varsome | rs387906389 |
LitVar | rs387906389 |
Map | rs387906389 |
PheGenI | rs387906389 |
Biobank | rs387906389 |
1000 genomes | rs387906389 |
hgdp | rs387906389 |
ensembl | rs387906389 |
geneview | rs387906389 |
scholar | rs387906389 |
rs387906389 | |
pharmgkb | rs387906389 |
gwascentral | rs387906389 |
openSNP | rs387906389 |
23andMe | rs387906389 |
SNPshot | rs387906389 |
SNPdbe | rs387906389 |
MSV3d | rs387906389 |
GWAS Ctlg | rs387906389 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906389(-;-) |
Alt | rs387906389(-;-) |
Reference | Rs387906389(GATGA;GATGA) |
Significance | Pathogenic |
Disease | Carcinoma of pancreas |
Variation | info |
Gene | ACVR1B |
CLNDBN | Carcinoma of pancreas |
Reversed | 0 |
HGVS | NC_000012.11:g.52380624_52380628delGATGA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000008710.4, |