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rs606231345

From SNPedia

Merged intors199769221
Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231345(A;A)
Make rs606231345(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position142751920
GenePRSS1
is asnp
is mentioned by
dbSNPrs606231345
ebirs606231345
HLIrs606231345
Exacrs606231345
Varsomers606231345
Maprs606231345
PheGenIrs606231345
hapmaprs606231345
1000 genomesrs606231345
hgdprs606231345
ensemblrs606231345
gopubmedrs606231345
geneviewrs606231345
scholarrs606231345
googlers606231345
pharmgkbrs606231345
gwascentralrs606231345
openSNPrs606231345
23andMers606231345
23andMe allrs606231345
SNP Nexus

SNPshotrs606231345
SNPdbers606231345
MSV3drs606231345
GWAS Ctlgrs606231345
StatusMerged into rs199769221
Max Magnitude0
ClinVar
Risk rs606231345(C;C)
Alt rs606231345(C;C)
Reference rs606231345(G;G)
Significance Probable-Pathogenic
Disease Hereditary pancreatitis
Variation info
Gene PRSS1
CLNDBN Hereditary pancreatitis
Reversed 0
HGVS NC_000007.14:g.142751920G>C
CLNSRC ClinVar
CLNACC RCV000149411.1,