rs77888940
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs77888940(C;G) |
Make rs77888940(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 1610017 |
Gene | FOXC1 |
is a | snp |
is | mentioned by |
dbSNP | rs77888940 |
dbSNP (classic) | rs77888940 |
ClinGen | rs77888940 |
ebi | rs77888940 |
HLI | rs77888940 |
Exac | rs77888940 |
Gnomad | rs77888940 |
Varsome | rs77888940 |
LitVar | rs77888940 |
Map | rs77888940 |
PheGenI | rs77888940 |
Biobank | rs77888940 |
1000 genomes | rs77888940 |
hgdp | rs77888940 |
ensembl | rs77888940 |
geneview | rs77888940 |
scholar | rs77888940 |
rs77888940 | |
pharmgkb | rs77888940 |
gwascentral | rs77888940 |
openSNP | rs77888940 |
23andMe | rs77888940 |
SNPshot | rs77888940 |
SNPdbe | rs77888940 |
MSV3d | rs77888940 |
GWAS Ctlg | rs77888940 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs77888940(G;G) |
Alt | rs77888940(G;G) |
Reference | Rs77888940(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FOXC1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.1610252C>G |
CLNSRC | |
CLNACC | RCV000162084.1, |