rs1064796288
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GG;GG) | 0 | common in clinvar |
Chromosome | 19 |
Position | 13025260 |
Gene | NFIX |
is a | snp |
is | mentioned by |
dbSNP | rs1064796288 |
dbSNP (classic) | rs1064796288 |
ClinGen | rs1064796288 |
ebi | rs1064796288 |
HLI | rs1064796288 |
Exac | rs1064796288 |
Gnomad | rs1064796288 |
Varsome | rs1064796288 |
LitVar | rs1064796288 |
Map | rs1064796288 |
PheGenI | rs1064796288 |
Biobank | rs1064796288 |
1000 genomes | rs1064796288 |
hgdp | rs1064796288 |
ensembl | rs1064796288 |
geneview | rs1064796288 |
scholar | rs1064796288 |
rs1064796288 | |
pharmgkb | rs1064796288 |
gwascentral | rs1064796288 |
openSNP | rs1064796288 |
23andMe | rs1064796288 |
SNPshot | rs1064796288 |
SNPdbe | rs1064796288 |
MSV3d | rs1064796288 |
GWAS Ctlg | rs1064796288 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064796288(C;C) |
Alt | rs1064796288(C;C) |
Reference | Rs1064796288(GG;GG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | NFIX |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.13136074_13136075delGGinsC |
CLNSRC | |
CLNACC | RCV000480113.1, |