rs1012472070
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1012472070(G;T) |
Make rs1012472070(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 88738367 |
Gene | LOC100289580, PIEZO1 |
is a | snp |
is | mentioned by |
dbSNP | rs1012472070 |
dbSNP (classic) | rs1012472070 |
ClinGen | rs1012472070 |
ebi | rs1012472070 |
HLI | rs1012472070 |
Exac | rs1012472070 |
Gnomad | rs1012472070 |
Varsome | rs1012472070 |
LitVar | rs1012472070 |
Map | rs1012472070 |
PheGenI | rs1012472070 |
Biobank | rs1012472070 |
1000 genomes | rs1012472070 |
hgdp | rs1012472070 |
ensembl | rs1012472070 |
geneview | rs1012472070 |
scholar | rs1012472070 |
rs1012472070 | |
pharmgkb | rs1012472070 |
gwascentral | rs1012472070 |
openSNP | rs1012472070 |
23andMe | rs1012472070 |
SNPshot | rs1012472070 |
SNPdbe | rs1012472070 |
MSV3d | rs1012472070 |
GWAS Ctlg | rs1012472070 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1012472070(A;A) rs1012472070(T;T) |
Alt | rs1012472070(A;A) rs1012472070(T;T) |
Reference | Rs1012472070(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.88804775G>T |
CLNSRC | |
CLNACC | RCV000479073.1, |