rs794727365
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs794727365(A;A) |
Make rs794727365(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 4 |
Position | 78364055 |
Gene | FRAS1 |
is a | snp |
is | mentioned by |
dbSNP | rs794727365 |
dbSNP (classic) | rs794727365 |
ClinGen | rs794727365 |
ebi | rs794727365 |
HLI | rs794727365 |
Exac | rs794727365 |
Gnomad | rs794727365 |
Varsome | rs794727365 |
LitVar | rs794727365 |
Map | rs794727365 |
PheGenI | rs794727365 |
Biobank | rs794727365 |
1000 genomes | rs794727365 |
hgdp | rs794727365 |
ensembl | rs794727365 |
geneview | rs794727365 |
scholar | rs794727365 |
rs794727365 | |
pharmgkb | rs794727365 |
gwascentral | rs794727365 |
openSNP | rs794727365 |
23andMe | rs794727365 |
SNPshot | rs794727365 |
SNPdbe | rs794727365 |
MSV3d | rs794727365 |
GWAS Ctlg | rs794727365 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794727365(A;A) |
Alt | rs794727365(A;A) |
Reference | Rs794727365(G;G) |
Significance | Pathogenic |
Disease | Cryptophthalmos syndrome not provided |
Variation | info |
Gene | FRAS1 |
CLNDBN | Cryptophthalmos syndrome not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.79285209G>A |
CLNSRC | |
CLNACC | RCV000176329.1, RCV000224135.1, |