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rs193922655

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922655(C;T)
Make rs193922655(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position142751962
GenePRSS1
is asnp
is mentioned by
dbSNPrs193922655
ebirs193922655
HLIrs193922655
Exacrs193922655
Varsomers193922655
Maprs193922655
PheGenIrs193922655
hapmaprs193922655
1000 genomesrs193922655
hgdprs193922655
ensemblrs193922655
gopubmedrs193922655
geneviewrs193922655
scholarrs193922655
googlers193922655
pharmgkbrs193922655
gwascentralrs193922655
openSNPrs193922655
23andMers193922655
23andMe allrs193922655
SNP Nexus

SNPshotrs193922655
SNPdbers193922655
MSV3drs193922655
GWAS Ctlgrs193922655
Max Magnitude0
ClinVar
Risk rs193922655(T;T)
Alt rs193922655(T;T)
Reference rs193922655(C;C)
Significance Probable-Pathogenic
Disease Hereditary pancreatitis
Variation info
Gene PRSS1
CLNDBN Hereditary pancreatitis
Reversed 0
HGVS NC_000007.13:g.142459813C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030383.1,