rs1064794737
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CGAGTGTGAACTTGTGAGTGTTCATTGCCT;CGAGTGTGAACTTGTGAGTGTTCATTGCCT) | 0 | common in clinvar |
Chromosome | 3 |
Position | 33051866 |
Gene | GLB1 |
is a | snp |
is | mentioned by |
dbSNP | rs1064794737 |
dbSNP (classic) | rs1064794737 |
ClinGen | rs1064794737 |
ebi | rs1064794737 |
HLI | rs1064794737 |
Exac | rs1064794737 |
Gnomad | rs1064794737 |
Varsome | rs1064794737 |
LitVar | rs1064794737 |
Map | rs1064794737 |
PheGenI | rs1064794737 |
Biobank | rs1064794737 |
1000 genomes | rs1064794737 |
hgdp | rs1064794737 |
ensembl | rs1064794737 |
geneview | rs1064794737 |
scholar | rs1064794737 |
rs1064794737 | |
pharmgkb | rs1064794737 |
gwascentral | rs1064794737 |
openSNP | rs1064794737 |
23andMe | rs1064794737 |
SNPshot | rs1064794737 |
SNPdbe | rs1064794737 |
MSV3d | rs1064794737 |
GWAS Ctlg | rs1064794737 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064794737(AGGCAAGTATATACTTGCC;AGGCAAGTATATACTTGCC) |
Alt | rs1064794737(AGGCAAGTATATACTTGCC;AGGCAAGTATATACTTGCC) |
Reference | Rs1064794737(CGAGTGTGAACTTGTGAGTGTTCATTGCCT;CGAGTGTGAACTTGTGAGTGTTCATTGCCT) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GLB1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000003.11:g.33093358_33093387del30insGGCAAGTATATACTTGCCT |
CLNSRC | |
CLNACC | RCV000479288.1, |