rs104895098
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs104895098(C;G) |
Make rs104895098(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 16 |
Position | 3243423 |
Gene | MEFV |
is a | snp |
is | mentioned by |
dbSNP | rs104895098 |
dbSNP (classic) | rs104895098 |
ClinGen | rs104895098 |
ebi | rs104895098 |
HLI | rs104895098 |
Exac | rs104895098 |
Gnomad | rs104895098 |
Varsome | rs104895098 |
LitVar | rs104895098 |
Map | rs104895098 |
PheGenI | rs104895098 |
Biobank | rs104895098 |
1000 genomes | rs104895098 |
hgdp | rs104895098 |
ensembl | rs104895098 |
geneview | rs104895098 |
scholar | rs104895098 |
rs104895098 | |
pharmgkb | rs104895098 |
gwascentral | rs104895098 |
openSNP | rs104895098 |
23andMe | rs104895098 |
SNPshot | rs104895098 |
SNPdbe | rs104895098 |
MSV3d | rs104895098 |
GWAS Ctlg | rs104895098 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104895098(G;G) |
Alt | rs104895098(G;G) |
Reference | Rs104895098(C;C) |
Significance | Pathogenic |
Disease | Familial Mediterranean fever |
Variation | info |
Gene | MEFV |
CLNDBN | Familial Mediterranean fever |
Reversed | 1 |
HGVS | NC_000016.9:g.3293423G>C |
CLNSRC | |
CLNACC | RCV000083736.1, |