rs1064795875
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1064795875(A;A) |
Make rs1064795875(A;G) |
Make rs1064795875(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 5 |
Position | 98902916 |
Gene | CHD1 |
is a | snp |
is | mentioned by |
dbSNP | rs1064795875 |
dbSNP (classic) | rs1064795875 |
ClinGen | rs1064795875 |
ebi | rs1064795875 |
HLI | rs1064795875 |
Exac | rs1064795875 |
Gnomad | rs1064795875 |
Varsome | rs1064795875 |
LitVar | rs1064795875 |
Map | rs1064795875 |
PheGenI | rs1064795875 |
Biobank | rs1064795875 |
1000 genomes | rs1064795875 |
hgdp | rs1064795875 |
ensembl | rs1064795875 |
geneview | rs1064795875 |
scholar | rs1064795875 |
rs1064795875 | |
pharmgkb | rs1064795875 |
gwascentral | rs1064795875 |
openSNP | rs1064795875 |
23andMe | rs1064795875 |
SNPshot | rs1064795875 |
SNPdbe | rs1064795875 |
MSV3d | rs1064795875 |
GWAS Ctlg | rs1064795875 |
Max Magnitude | 0 |
OMIM pathogenic