rs1064796408
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;CGCGGCCCGTGCTG) | 7 | Von Hippel-Lindau syndrome mutation |
(GGCCCGTGCTGCGC;GGCCCGTGCTGCGC) | 0 | common/normal |
Make rs1064796408(-;-) |
Make rs1064796408(-;GGCCCGTGCTGCGC) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 3 |
Position | 10142026 |
Gene | VHL |
is a | snp |
is | mentioned by |
dbSNP | rs1064796408 |
dbSNP (classic) | rs1064796408 |
ClinGen | rs1064796408 |
ebi | rs1064796408 |
HLI | rs1064796408 |
Exac | rs1064796408 |
Gnomad | rs1064796408 |
Varsome | rs1064796408 |
LitVar | rs1064796408 |
Map | rs1064796408 |
PheGenI | rs1064796408 |
Biobank | rs1064796408 |
1000 genomes | rs1064796408 |
hgdp | rs1064796408 |
ensembl | rs1064796408 |
geneview | rs1064796408 |
scholar | rs1064796408 |
rs1064796408 | |
pharmgkb | rs1064796408 |
gwascentral | rs1064796408 |
openSNP | rs1064796408 |
23andMe | rs1064796408 |
SNPshot | rs1064796408 |
SNPdbe | rs1064796408 |
MSV3d | rs1064796408 |
GWAS Ctlg | rs1064796408 |
Max Magnitude | 7 |