rs754404446
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs754404446(A;A) |
Make rs754404446(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 128242281 |
Gene | DNM1 |
is a | snp |
is | mentioned by |
dbSNP | rs754404446 |
dbSNP (classic) | rs754404446 |
ClinGen | rs754404446 |
ebi | rs754404446 |
HLI | rs754404446 |
Exac | rs754404446 |
Gnomad | rs754404446 |
Varsome | rs754404446 |
LitVar | rs754404446 |
Map | rs754404446 |
PheGenI | rs754404446 |
Biobank | rs754404446 |
1000 genomes | rs754404446 |
hgdp | rs754404446 |
ensembl | rs754404446 |
geneview | rs754404446 |
scholar | rs754404446 |
rs754404446 | |
pharmgkb | rs754404446 |
gwascentral | rs754404446 |
openSNP | rs754404446 |
23andMe | rs754404446 |
SNPshot | rs754404446 |
SNPdbe | rs754404446 |
MSV3d | rs754404446 |
GWAS Ctlg | rs754404446 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs754404446(A;A) rs754404446(C;C) |
Alt | rs754404446(A;A) rs754404446(C;C) |
Reference | Rs754404446(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DNM1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.131004560G>A |
CLNSRC | |
CLNACC | RCV000413377.1, |