rs1057518107
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TT;TT) | 0 | common in clinvar |
Make rs1057518107(-;-) |
Make rs1057518107(-;TT) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 7561047 |
Gene | PNPLA6 |
is a | snp |
is | mentioned by |
dbSNP | rs1057518107 |
dbSNP (classic) | rs1057518107 |
ClinGen | rs1057518107 |
ebi | rs1057518107 |
HLI | rs1057518107 |
Exac | rs1057518107 |
Gnomad | rs1057518107 |
Varsome | rs1057518107 |
LitVar | rs1057518107 |
Map | rs1057518107 |
PheGenI | rs1057518107 |
Biobank | rs1057518107 |
1000 genomes | rs1057518107 |
hgdp | rs1057518107 |
ensembl | rs1057518107 |
geneview | rs1057518107 |
scholar | rs1057518107 |
rs1057518107 | |
pharmgkb | rs1057518107 |
gwascentral | rs1057518107 |
openSNP | rs1057518107 |
23andMe | rs1057518107 |
SNPshot | rs1057518107 |
SNPdbe | rs1057518107 |
MSV3d | rs1057518107 |
GWAS Ctlg | rs1057518107 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057518107(-;-) |
Alt | rs1057518107(-;-) |
Reference | Rs1057518107(TT;TT) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PNPLA6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.7625933_7625934delTT |
CLNSRC | |
CLNACC | RCV000413299.1, |