rs1076165
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1076165(A;A) |
Make rs1076165(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 2870106 |
Gene | RAP1GAP2 |
is a | snp |
is | mentioned by |
dbSNP | rs1076165 |
dbSNP (classic) | rs1076165 |
ClinGen | rs1076165 |
ebi | rs1076165 |
HLI | rs1076165 |
Exac | rs1076165 |
Gnomad | rs1076165 |
Varsome | rs1076165 |
LitVar | rs1076165 |
Map | rs1076165 |
PheGenI | rs1076165 |
Biobank | rs1076165 |
1000 genomes | rs1076165 |
hgdp | rs1076165 |
ensembl | rs1076165 |
geneview | rs1076165 |
scholar | rs1076165 |
rs1076165 | |
pharmgkb | rs1076165 |
gwascentral | rs1076165 |
openSNP | rs1076165 |
23andMe | rs1076165 |
SNPshot | rs1076165 |
SNPdbe | rs1076165 |
MSV3d | rs1076165 |
GWAS Ctlg | rs1076165 |
GMAF | 0.2222 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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