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rs387906698

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906698(C;T)
Make rs387906698(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position142751919
GenePRSS1
is asnp
is mentioned by
dbSNPrs387906698
ebirs387906698
HLIrs387906698
Exacrs387906698
Varsomers387906698
Maprs387906698
PheGenIrs387906698
hapmaprs387906698
1000 genomesrs387906698
hgdprs387906698
ensemblrs387906698
gopubmedrs387906698
geneviewrs387906698
scholarrs387906698
googlers387906698
pharmgkbrs387906698
gwascentralrs387906698
openSNPrs387906698
23andMers387906698
23andMe allrs387906698
SNP Nexus

SNPshotrs387906698
SNPdbers387906698
MSV3drs387906698
GWAS Ctlgrs387906698
Max Magnitude0
ClinVar
Risk rs387906698(T;T)
Alt rs387906698(T;T)
Reference rs387906698(C;C)
Significance Pathogenic
Disease Hereditary pancreatitis
Variation info
Gene PRSS1
CLNDBN Hereditary pancreatitis
Reversed 0
HGVS NC_000007.13:g.142459770C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022814.22,