rs558274487
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs558274487(A;A) |
Make rs558274487(A;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 127939952 |
Gene | MFSD8 |
is a | snp |
is | mentioned by |
dbSNP | rs558274487 |
dbSNP (classic) | rs558274487 |
ClinGen | rs558274487 |
ebi | rs558274487 |
HLI | rs558274487 |
Exac | rs558274487 |
Gnomad | rs558274487 |
Varsome | rs558274487 |
LitVar | rs558274487 |
Map | rs558274487 |
PheGenI | rs558274487 |
Biobank | rs558274487 |
1000 genomes | rs558274487 |
hgdp | rs558274487 |
ensembl | rs558274487 |
geneview | rs558274487 |
scholar | rs558274487 |
rs558274487 | |
pharmgkb | rs558274487 |
gwascentral | rs558274487 |
openSNP | rs558274487 |
23andMe | rs558274487 |
SNPshot | rs558274487 |
SNPdbe | rs558274487 |
MSV3d | rs558274487 |
GWAS Ctlg | rs558274487 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs558274487(A;A) rs558274487(T;T) |
Alt | rs558274487(A;A) rs558274487(T;T) |
Reference | Rs558274487(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MFSD8 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.128861107C>T |
CLNSRC | |
CLNACC | RCV000188167.1, |