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rs515726208

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs515726208(A;A)
Make rs515726208(A;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position147824702
GeneSPINK1
is asnp
is mentioned by
dbSNPrs515726208
ebirs515726208
HLIrs515726208
Exacrs515726208
Varsomers515726208
Maprs515726208
PheGenIrs515726208
hapmaprs515726208
1000 genomesrs515726208
hgdprs515726208
ensemblrs515726208
gopubmedrs515726208
geneviewrs515726208
scholarrs515726208
googlers515726208
pharmgkbrs515726208
gwascentralrs515726208
openSNPrs515726208
23andMers515726208
23andMe allrs515726208
SNP Nexus

SNPshotrs515726208
SNPdbers515726208
MSV3drs515726208
GWAS Ctlgrs515726208
Max Magnitude0
ClinVar
Risk rs515726208(A;A)
Alt rs515726208(A;A)
Reference rs515726208(G;G)
Significance Pathogenic
Disease Hereditary pancreatitis
Variation info
Gene SPINK1
CLNDBN Hereditary pancreatitis
Reversed 0
HGVS NC_000005.9:g.147204265G>A
CLNSRC ClinVar
CLNACC RCV000119034.2,