Have questions? Visit https://www.reddit.com/r/SNPedia

rs199769221

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199769221(A;A)
Make rs199769221(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position142751920
GenePRSS1
is asnp
is mentioned by
dbSNPrs199769221
ebirs199769221
HLIrs199769221
Exacrs199769221
Varsomers199769221
Maprs199769221
PheGenIrs199769221
hapmaprs199769221
1000 genomesrs199769221
hgdprs199769221
ensemblrs199769221
gopubmedrs199769221
geneviewrs199769221
scholarrs199769221
googlers199769221
pharmgkbrs199769221
gwascentralrs199769221
openSNPrs199769221
23andMers199769221
23andMe allrs199769221
SNP Nexus

SNPshotrs199769221
SNPdbers199769221
MSV3drs199769221
GWAS Ctlgrs199769221
Merged fromRs606231345
Max Magnitude0
ClinVar
Risk rs199769221(A,C,T;A,C,T)
Alt rs199769221(A,C,T;A,C,T)
Reference rs199769221(G;G)
Significance Probable-Pathogenic
Disease Hereditary pancreatitis
Variation info
Gene PRSS1
CLNDBN Hereditary pancreatitis
Reversed 0
HGVS NC_000007.13:g.142459771G>C
CLNSRC
CLNACC RCV000149411.1,