rs1057519025
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1057519025(AT;AT) |
Make rs1057519025(AT;TC) |
Make rs1057519025(TC;TC) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 12 |
Position | 7091533 |
Gene | C1R |
is a | snp |
is | mentioned by |
dbSNP | rs1057519025 |
dbSNP (classic) | rs1057519025 |
ClinGen | rs1057519025 |
ebi | rs1057519025 |
HLI | rs1057519025 |
Exac | rs1057519025 |
Gnomad | rs1057519025 |
Varsome | rs1057519025 |
LitVar | rs1057519025 |
Map | rs1057519025 |
PheGenI | rs1057519025 |
Biobank | rs1057519025 |
1000 genomes | rs1057519025 |
hgdp | rs1057519025 |
ensembl | rs1057519025 |
geneview | rs1057519025 |
scholar | rs1057519025 |
rs1057519025 | |
pharmgkb | rs1057519025 |
gwascentral | rs1057519025 |
openSNP | rs1057519025 |
23andMe | rs1057519025 |
SNPshot | rs1057519025 |
SNPdbe | rs1057519025 |
MSV3d | rs1057519025 |
GWAS Ctlg | rs1057519025 |
Max Magnitude | 0 |
OMIM pathogenic