rs1057517758
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1057517758(A;A) |
Make rs1057517758(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 90556586 |
Gene | MAP3K7 |
is a | snp |
is | mentioned by |
dbSNP | rs1057517758 |
dbSNP (old) | rs1057517758 |
ClinGen | rs1057517758 |
ebi | rs1057517758 |
HLI | rs1057517758 |
Exac | rs1057517758 |
Gnomad | rs1057517758 |
Varsome | rs1057517758 |
Map | rs1057517758 |
PheGenI | rs1057517758 |
Biobank | rs1057517758 |
1000 genomes | rs1057517758 |
hgdp | rs1057517758 |
ensembl | rs1057517758 |
gopubmed | rs1057517758 |
geneview | rs1057517758 |
scholar | rs1057517758 |
rs1057517758 | |
pharmgkb | rs1057517758 |
gwascentral | rs1057517758 |
openSNP | rs1057517758 |
23andMe | rs1057517758 |
23andMe all | rs1057517758 |
SNPshot | rs1057517758 |
SNPdbe | rs1057517758 |
MSV3d | rs1057517758 |
GWAS Ctlg | rs1057517758 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057517758(A;A) |
Alt | rs1057517758(A;A) |
Reference | Rs1057517758(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MAP3K7 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000006.11:g.91266305C>T |
CLNSRC | |
CLNACC | RCV000414538.1, |