rs199769221
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs199769221(A;A) |
Make rs199769221(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 7 |
Position | 142751920 |
Gene | PRSS1 |
is a | snp |
is | mentioned by |
dbSNP | rs199769221 |
dbSNP (classic) | rs199769221 |
ClinGen | rs199769221 |
ebi | rs199769221 |
HLI | rs199769221 |
Exac | rs199769221 |
Gnomad | rs199769221 |
Varsome | rs199769221 |
LitVar | rs199769221 |
Map | rs199769221 |
PheGenI | rs199769221 |
Biobank | rs199769221 |
1000 genomes | rs199769221 |
hgdp | rs199769221 |
ensembl | rs199769221 |
geneview | rs199769221 |
scholar | rs199769221 |
rs199769221 | |
pharmgkb | rs199769221 |
gwascentral | rs199769221 |
openSNP | rs199769221 |
23andMe | rs199769221 |
SNPshot | rs199769221 |
SNPdbe | rs199769221 |
MSV3d | rs199769221 |
GWAS Ctlg | rs199769221 |
Merged from | Rs606231345 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199769221(A;A) rs199769221(C;C) rs199769221(T;T) |
Alt | rs199769221(A;A) rs199769221(C;C) rs199769221(T;T) |
Reference | Rs199769221(G;G) |
Significance | Probable-Pathogenic |
Disease | Hereditary pancreatitis |
Variation | info |
Gene | PRSS1 |
CLNDBN | Hereditary pancreatitis |
Reversed | 0 |
HGVS | NC_000007.13:g.142459771G>C |
CLNSRC | |
CLNACC | RCV000149411.1, |