rs9907627
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs9907627(A;A) |
Make rs9907627(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 31232140 |
Gene | NF1 |
is a | snp |
is | mentioned by |
dbSNP | rs9907627 |
dbSNP (classic) | rs9907627 |
ClinGen | rs9907627 |
ebi | rs9907627 |
HLI | rs9907627 |
Exac | rs9907627 |
Gnomad | rs9907627 |
Varsome | rs9907627 |
LitVar | rs9907627 |
Map | rs9907627 |
PheGenI | rs9907627 |
Biobank | rs9907627 |
1000 genomes | rs9907627 |
hgdp | rs9907627 |
ensembl | rs9907627 |
geneview | rs9907627 |
scholar | rs9907627 |
rs9907627 | |
pharmgkb | rs9907627 |
gwascentral | rs9907627 |
openSNP | rs9907627 |
23andMe | rs9907627 |
SNPshot | rs9907627 |
SNPdbe | rs9907627 |
MSV3d | rs9907627 |
GWAS Ctlg | rs9907627 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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