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rs515726206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs515726206(A;C)
Make rs515726206(C;C)
ReferenceGRCh38 38.1/142
Chromosome5
Position147828066
GeneSPINK1
is asnp
is mentioned by
dbSNPrs515726206
ebirs515726206
HLIrs515726206
Exacrs515726206
Varsomers515726206
Maprs515726206
PheGenIrs515726206
hapmaprs515726206
1000 genomesrs515726206
hgdprs515726206
ensemblrs515726206
gopubmedrs515726206
geneviewrs515726206
scholarrs515726206
googlers515726206
pharmgkbrs515726206
gwascentralrs515726206
openSNPrs515726206
23andMers515726206
23andMe allrs515726206
SNP Nexus

SNPshotrs515726206
SNPdbers515726206
MSV3drs515726206
GWAS Ctlgrs515726206
Max Magnitude0
ClinVar
Risk rs515726206(C;C)
Alt rs515726206(C;C)
Reference rs515726206(A;A)
Significance Pathogenic
Disease Hereditary pancreatitis
Variation info
Gene SPINK1
CLNDBN Hereditary pancreatitis
Reversed 0
HGVS NC_000005.9:g.147207629A>C
CLNSRC ClinVar
CLNACC RCV000119032.2,