rs1028250483
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1028250483(C;T) |
Make rs1028250483(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 156175179 |
Gene | SEMA4A |
is a | snp |
is | mentioned by |
dbSNP | rs1028250483 |
dbSNP (classic) | rs1028250483 |
ClinGen | rs1028250483 |
ebi | rs1028250483 |
HLI | rs1028250483 |
Exac | rs1028250483 |
Gnomad | rs1028250483 |
Varsome | rs1028250483 |
LitVar | rs1028250483 |
Map | rs1028250483 |
PheGenI | rs1028250483 |
Biobank | rs1028250483 |
1000 genomes | rs1028250483 |
hgdp | rs1028250483 |
ensembl | rs1028250483 |
geneview | rs1028250483 |
scholar | rs1028250483 |
rs1028250483 | |
pharmgkb | rs1028250483 |
gwascentral | rs1028250483 |
openSNP | rs1028250483 |
23andMe | rs1028250483 |
SNPshot | rs1028250483 |
SNPdbe | rs1028250483 |
MSV3d | rs1028250483 |
GWAS Ctlg | rs1028250483 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1028250483(T;T) |
Alt | rs1028250483(T;T) |
Reference | Rs1028250483(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SEMA4A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.156144970C>T |
CLNSRC | |
CLNACC | RCV000437436.1, |