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rs267606982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs267606982(AT;AT)
Make rs267606982(AT;GC)
ReferenceGRCh38 38.1/141
Chromosome7
Position142751938
GenePRSS1
is asnp
is mentioned by
dbSNPrs267606982
ebirs267606982
HLIrs267606982
Exacrs267606982
Varsomers267606982
Maprs267606982
PheGenIrs267606982
hapmaprs267606982
1000 genomesrs267606982
hgdprs267606982
ensemblrs267606982
gopubmedrs267606982
geneviewrs267606982
scholarrs267606982
googlers267606982
pharmgkbrs267606982
gwascentralrs267606982
openSNPrs267606982
23andMers267606982
23andMe allrs267606982
SNP Nexus

SNPshotrs267606982
SNPdbers267606982
MSV3drs267606982
GWAS Ctlgrs267606982
Max Magnitude0
ClinVar
Risk rs267606982(AT;AT)
Alt rs267606982(AT;AT)
Reference rs267606982(GC;GC)
Significance Pathogenic
Disease Hereditary pancreatitis
Variation info
Gene PRSS1
CLNDBN Hereditary pancreatitis
Reversed 0
HGVS NC_000007.13:g.142459789_142459790delGCinsAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000012657.25,