rs1064794624
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Chromosome | 22 |
Position | 41169518 |
is a | snp |
is | mentioned by |
dbSNP | rs1064794624 |
dbSNP (classic) | rs1064794624 |
ClinGen | rs1064794624 |
ebi | rs1064794624 |
HLI | rs1064794624 |
Exac | rs1064794624 |
Gnomad | rs1064794624 |
Varsome | rs1064794624 |
LitVar | rs1064794624 |
Map | rs1064794624 |
PheGenI | rs1064794624 |
Biobank | rs1064794624 |
1000 genomes | rs1064794624 |
hgdp | rs1064794624 |
ensembl | rs1064794624 |
geneview | rs1064794624 |
scholar | rs1064794624 |
rs1064794624 | |
pharmgkb | rs1064794624 |
gwascentral | rs1064794624 |
openSNP | rs1064794624 |
23andMe | rs1064794624 |
SNPshot | rs1064794624 |
SNPdbe | rs1064794624 |
MSV3d | rs1064794624 |
GWAS Ctlg | rs1064794624 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064794624(CCTATGTATATCTCCTATACATATCTCCTATCGAACA;CCTATGTATATCTCCTATACATATCTCCTATCGAACA) |
Alt | rs1064794624(CCTATGTATATCTCCTATACATATCTCCTATCGAACA;CCTATGTATATCTCCTATACATATCTCCTATCGAACA) |
Reference | Rs1064794624(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.41565522_41565523insCCTATGTATATCTCCTATACATATCTCCTATCGAACA |
CLNSRC | |
CLNACC | RCV000487041.1, |