rs1064793754
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AAGT;AAGT) | 0 | common in clinvar |
Chromosome | 1 |
Position | 108922579 |
Gene | GPSM2 |
is a | snp |
is | mentioned by |
dbSNP | rs1064793754 |
dbSNP (classic) | rs1064793754 |
ClinGen | rs1064793754 |
ebi | rs1064793754 |
HLI | rs1064793754 |
Exac | rs1064793754 |
Gnomad | rs1064793754 |
Varsome | rs1064793754 |
LitVar | rs1064793754 |
Map | rs1064793754 |
PheGenI | rs1064793754 |
Biobank | rs1064793754 |
1000 genomes | rs1064793754 |
hgdp | rs1064793754 |
ensembl | rs1064793754 |
geneview | rs1064793754 |
scholar | rs1064793754 |
rs1064793754 | |
pharmgkb | rs1064793754 |
gwascentral | rs1064793754 |
openSNP | rs1064793754 |
23andMe | rs1064793754 |
SNPshot | rs1064793754 |
SNPdbe | rs1064793754 |
MSV3d | rs1064793754 |
GWAS Ctlg | rs1064793754 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064793754(-;-) |
Alt | rs1064793754(-;-) |
Reference | Rs1064793754(AAGT;AAGT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | GPSM2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.109465201_109465204delAAGT |
CLNSRC | |
CLNACC | RCV000487382.1, |