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rs193922656

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922656(C;G)
Make rs193922656(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position142751971
GenePRSS1
is asnp
is mentioned by
dbSNPrs193922656
ebirs193922656
HLIrs193922656
Exacrs193922656
Varsomers193922656
Maprs193922656
PheGenIrs193922656
hapmaprs193922656
1000 genomesrs193922656
hgdprs193922656
ensemblrs193922656
gopubmedrs193922656
geneviewrs193922656
scholarrs193922656
googlers193922656
pharmgkbrs193922656
gwascentralrs193922656
openSNPrs193922656
23andMers193922656
23andMe allrs193922656
SNP Nexus

SNPshotrs193922656
SNPdbers193922656
MSV3drs193922656
GWAS Ctlgrs193922656
Max Magnitude0
ClinVar
Risk rs193922656(G;G)
Alt rs193922656(G;G)
Reference rs193922656(C;C)
Significance Probable-Pathogenic
Disease Hereditary pancreatitis
Variation info
Gene PRSS1
CLNDBN Hereditary pancreatitis
Reversed 0
HGVS NC_000007.13:g.142459822C>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030384.1,