rs1220533001
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;G) | 3 | Carrier of a tumoral calcinosis mutation |
Make rs1220533001(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 12 |
Position | 4370732 |
Gene | FGF23 |
is a | snp |
is | mentioned by |
dbSNP | rs1220533001 |
dbSNP (classic) | rs1220533001 |
ClinGen | rs1220533001 |
ebi | rs1220533001 |
HLI | rs1220533001 |
Exac | rs1220533001 |
Gnomad | rs1220533001 |
Varsome | rs1220533001 |
LitVar | rs1220533001 |
Map | rs1220533001 |
PheGenI | rs1220533001 |
Biobank | rs1220533001 |
1000 genomes | rs1220533001 |
hgdp | rs1220533001 |
ensembl | rs1220533001 |
geneview | rs1220533001 |
scholar | rs1220533001 |
rs1220533001 | |
pharmgkb | rs1220533001 |
gwascentral | rs1220533001 |
openSNP | rs1220533001 |
23andMe | rs1220533001 |
SNPshot | rs1220533001 |
SNPdbe | rs1220533001 |
MSV3d | rs1220533001 |
GWAS Ctlg | rs1220533001 |
Max Magnitude | 3 |
aka c.367G>T (p.Gly123Trp or G123W)