rs772219642
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs772219642(G;T) |
Make rs772219642(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 180619298 |
Gene | CCDC39 |
is a | snp |
is | mentioned by |
dbSNP | rs772219642 |
dbSNP (classic) | rs772219642 |
ClinGen | rs772219642 |
ebi | rs772219642 |
HLI | rs772219642 |
Exac | rs772219642 |
Gnomad | rs772219642 |
Varsome | rs772219642 |
LitVar | rs772219642 |
Map | rs772219642 |
PheGenI | rs772219642 |
Biobank | rs772219642 |
1000 genomes | rs772219642 |
hgdp | rs772219642 |
ensembl | rs772219642 |
geneview | rs772219642 |
scholar | rs772219642 |
rs772219642 | |
pharmgkb | rs772219642 |
gwascentral | rs772219642 |
openSNP | rs772219642 |
23andMe | rs772219642 |
SNPshot | rs772219642 |
SNPdbe | rs772219642 |
MSV3d | rs772219642 |
GWAS Ctlg | rs772219642 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772219642(T;T) |
Alt | rs772219642(T;T) |
Reference | Rs772219642(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CCDC39 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.180337086G>T |
CLNSRC | |
CLNACC | RCV000479757.1, |