rs143511416
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs143511416(C;T) |
Make rs143511416(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 196217066 |
Gene | HECW2 |
is a | snp |
is | mentioned by |
dbSNP | rs143511416 |
dbSNP (classic) | rs143511416 |
ClinGen | rs143511416 |
ebi | rs143511416 |
HLI | rs143511416 |
Exac | rs143511416 |
Gnomad | rs143511416 |
Varsome | rs143511416 |
LitVar | rs143511416 |
Map | rs143511416 |
PheGenI | rs143511416 |
Biobank | rs143511416 |
1000 genomes | rs143511416 |
hgdp | rs143511416 |
ensembl | rs143511416 |
geneview | rs143511416 |
scholar | rs143511416 |
rs143511416 | |
pharmgkb | rs143511416 |
gwascentral | rs143511416 |
openSNP | rs143511416 |
23andMe | rs143511416 |
SNPshot | rs143511416 |
SNPdbe | rs143511416 |
MSV3d | rs143511416 |
GWAS Ctlg | rs143511416 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs143511416(T;T) |
Alt | rs143511416(T;T) |
Reference | Rs143511416(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | HECW2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.197081790C>T |
CLNSRC | |
CLNACC | RCV000442124.1, |