rs748155949
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs748155949(C;C) |
Make rs748155949(C;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 88731721 |
Gene | LOC100289580, PIEZO1 |
is a | snp |
is | mentioned by |
dbSNP | rs748155949 |
dbSNP (classic) | rs748155949 |
ClinGen | rs748155949 |
ebi | rs748155949 |
HLI | rs748155949 |
Exac | rs748155949 |
Gnomad | rs748155949 |
Varsome | rs748155949 |
LitVar | rs748155949 |
Map | rs748155949 |
PheGenI | rs748155949 |
Biobank | rs748155949 |
1000 genomes | rs748155949 |
hgdp | rs748155949 |
ensembl | rs748155949 |
geneview | rs748155949 |
scholar | rs748155949 |
rs748155949 | |
pharmgkb | rs748155949 |
gwascentral | rs748155949 |
openSNP | rs748155949 |
23andMe | rs748155949 |
SNPshot | rs748155949 |
SNPdbe | rs748155949 |
MSV3d | rs748155949 |
GWAS Ctlg | rs748155949 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs748155949(C;C) |
Alt | rs748155949(C;C) |
Reference | Rs748155949(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LOC100289580 PIEZO1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.88798129G>C |
CLNSRC | |
CLNACC | RCV000490090.1, |