rs1064797030
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GC;GC) | 0 | common in clinvar |
Chromosome | 14 |
Position | 28767864 |
Gene | FOXG1 |
is a | snp |
is | mentioned by |
dbSNP | rs1064797030 |
dbSNP (classic) | rs1064797030 |
ClinGen | rs1064797030 |
ebi | rs1064797030 |
HLI | rs1064797030 |
Exac | rs1064797030 |
Gnomad | rs1064797030 |
Varsome | rs1064797030 |
LitVar | rs1064797030 |
Map | rs1064797030 |
PheGenI | rs1064797030 |
Biobank | rs1064797030 |
1000 genomes | rs1064797030 |
hgdp | rs1064797030 |
ensembl | rs1064797030 |
geneview | rs1064797030 |
scholar | rs1064797030 |
rs1064797030 | |
pharmgkb | rs1064797030 |
gwascentral | rs1064797030 |
openSNP | rs1064797030 |
23andMe | rs1064797030 |
SNPshot | rs1064797030 |
SNPdbe | rs1064797030 |
MSV3d | rs1064797030 |
GWAS Ctlg | rs1064797030 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064797030(TT;TT) |
Alt | rs1064797030(TT;TT) |
Reference | Rs1064797030(GC;GC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FOXG1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.29237070_29237071delGCinsTT |
CLNSRC | |
CLNACC | RCV000480058.1, |