rs1010078101
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1010078101(A;A) |
Make rs1010078101(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 19665042 |
Gene | ALDH3A2 |
is a | snp |
is | mentioned by |
dbSNP | rs1010078101 |
dbSNP (classic) | rs1010078101 |
ClinGen | rs1010078101 |
ebi | rs1010078101 |
HLI | rs1010078101 |
Exac | rs1010078101 |
Gnomad | rs1010078101 |
Varsome | rs1010078101 |
LitVar | rs1010078101 |
Map | rs1010078101 |
PheGenI | rs1010078101 |
Biobank | rs1010078101 |
1000 genomes | rs1010078101 |
hgdp | rs1010078101 |
ensembl | rs1010078101 |
geneview | rs1010078101 |
scholar | rs1010078101 |
rs1010078101 | |
pharmgkb | rs1010078101 |
gwascentral | rs1010078101 |
openSNP | rs1010078101 |
23andMe | rs1010078101 |
SNPshot | rs1010078101 |
SNPdbe | rs1010078101 |
MSV3d | rs1010078101 |
GWAS Ctlg | rs1010078101 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1010078101(A;A) |
Alt | rs1010078101(A;A) |
Reference | Rs1010078101(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ALDH3A2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.19568355G>A |
CLNSRC | |
CLNACC | RCV000437687.1, |