rs141476300
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs141476300(A;A) |
Make rs141476300(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 45979728 |
Gene | FYCO1 |
is a | snp |
is | mentioned by |
dbSNP | rs141476300 |
dbSNP (classic) | rs141476300 |
ClinGen | rs141476300 |
ebi | rs141476300 |
HLI | rs141476300 |
Exac | rs141476300 |
Gnomad | rs141476300 |
Varsome | rs141476300 |
LitVar | rs141476300 |
Map | rs141476300 |
PheGenI | rs141476300 |
Biobank | rs141476300 |
1000 genomes | rs141476300 |
hgdp | rs141476300 |
ensembl | rs141476300 |
geneview | rs141476300 |
scholar | rs141476300 |
rs141476300 | |
pharmgkb | rs141476300 |
gwascentral | rs141476300 |
openSNP | rs141476300 |
23andMe | rs141476300 |
SNPshot | rs141476300 |
SNPdbe | rs141476300 |
MSV3d | rs141476300 |
GWAS Ctlg | rs141476300 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141476300(A;A) |
Alt | rs141476300(A;A) |
Reference | Rs141476300(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | FYCO1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.46021220G>A |
CLNSRC | |
CLNACC | RCV000488185.1, |