rs606231383
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs606231383(-;C) |
Make rs606231383(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 18868806 |
Gene | CERS1, GDF1 |
is a | snp |
is | mentioned by |
dbSNP | rs606231383 |
dbSNP (classic) | rs606231383 |
ClinGen | rs606231383 |
ebi | rs606231383 |
HLI | rs606231383 |
Exac | rs606231383 |
Gnomad | rs606231383 |
Varsome | rs606231383 |
LitVar | rs606231383 |
Map | rs606231383 |
PheGenI | rs606231383 |
Biobank | rs606231383 |
1000 genomes | rs606231383 |
hgdp | rs606231383 |
ensembl | rs606231383 |
geneview | rs606231383 |
scholar | rs606231383 |
rs606231383 | |
pharmgkb | rs606231383 |
gwascentral | rs606231383 |
openSNP | rs606231383 |
23andMe | rs606231383 |
SNPshot | rs606231383 |
SNPdbe | rs606231383 |
MSV3d | rs606231383 |
GWAS Ctlg | rs606231383 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs606231383(C;C) |
Alt | rs606231383(C;C) |
Reference | Rs606231383(-;-) |
Significance | Pathogenic |
Disease | Bilateral right-sidedness sequence |
Variation | info |
Gene | CERS1 GDF1 |
CLNDBN | Bilateral right-sidedness sequence |
Reversed | 1 |
HGVS | NC_000019.9:g.18979616dupG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000055616.3, |