rs55830907
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs55830907(C;T) |
Make rs55830907(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 161360169 |
Gene | PARK2 |
is a | snp |
is | mentioned by |
dbSNP | rs55830907 |
dbSNP (classic) | rs55830907 |
ClinGen | rs55830907 |
ebi | rs55830907 |
HLI | rs55830907 |
Exac | rs55830907 |
Gnomad | rs55830907 |
Varsome | rs55830907 |
LitVar | rs55830907 |
Map | rs55830907 |
PheGenI | rs55830907 |
Biobank | rs55830907 |
1000 genomes | rs55830907 |
hgdp | rs55830907 |
ensembl | rs55830907 |
geneview | rs55830907 |
scholar | rs55830907 |
rs55830907 | |
pharmgkb | rs55830907 |
gwascentral | rs55830907 |
openSNP | rs55830907 |
23andMe | rs55830907 |
SNPshot | rs55830907 |
SNPdbe | rs55830907 |
MSV3d | rs55830907 |
GWAS Ctlg | rs55830907 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs55830907(T;T) |
Alt | rs55830907(T;T) |
Reference | Rs55830907(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | PARK2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000006.11:g.161781201G>A |
CLNSRC | |
CLNACC | RCV000487928.1, |