rs371610471
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs371610471(C;T) |
Make rs371610471(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 136327158 |
Gene | PCCB |
is a | snp |
is | mentioned by |
dbSNP | rs371610471 |
dbSNP (classic) | rs371610471 |
ClinGen | rs371610471 |
ebi | rs371610471 |
HLI | rs371610471 |
Exac | rs371610471 |
Gnomad | rs371610471 |
Varsome | rs371610471 |
LitVar | rs371610471 |
Map | rs371610471 |
PheGenI | rs371610471 |
Biobank | rs371610471 |
1000 genomes | rs371610471 |
hgdp | rs371610471 |
ensembl | rs371610471 |
geneview | rs371610471 |
scholar | rs371610471 |
rs371610471 | |
pharmgkb | rs371610471 |
gwascentral | rs371610471 |
openSNP | rs371610471 |
23andMe | rs371610471 |
SNPshot | rs371610471 |
SNPdbe | rs371610471 |
MSV3d | rs371610471 |
GWAS Ctlg | rs371610471 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs371610471(T;T) |
Alt | rs371610471(T;T) |
Reference | Rs371610471(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PCCB |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.136046000C>A |
CLNSRC | |
CLNACC | RCV000186090.1, |