rs559155109
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs559155109(A;G) |
Make rs559155109(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 4 |
Position | 127920826 |
Gene | MFSD8 |
is a | snp |
is | mentioned by |
dbSNP | rs559155109 |
dbSNP (classic) | rs559155109 |
ClinGen | rs559155109 |
ebi | rs559155109 |
HLI | rs559155109 |
Exac | rs559155109 |
Gnomad | rs559155109 |
Varsome | rs559155109 |
LitVar | rs559155109 |
Map | rs559155109 |
PheGenI | rs559155109 |
Biobank | rs559155109 |
1000 genomes | rs559155109 |
hgdp | rs559155109 |
ensembl | rs559155109 |
geneview | rs559155109 |
scholar | rs559155109 |
rs559155109 | |
pharmgkb | rs559155109 |
gwascentral | rs559155109 |
openSNP | rs559155109 |
23andMe | rs559155109 |
SNPshot | rs559155109 |
SNPdbe | rs559155109 |
MSV3d | rs559155109 |
GWAS Ctlg | rs559155109 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs559155109(G;G) |
Alt | rs559155109(G;G) |
Reference | Rs559155109(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MFSD8 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.128841981A>G |
CLNSRC | |
CLNACC | RCV000480079.1, |