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rs515726207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs515726207(A;G)
Make rs515726207(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position147828056
GeneSPINK1
is asnp
is mentioned by
dbSNPrs515726207
ebirs515726207
HLIrs515726207
Exacrs515726207
Varsomers515726207
Maprs515726207
PheGenIrs515726207
hapmaprs515726207
1000 genomesrs515726207
hgdprs515726207
ensemblrs515726207
gopubmedrs515726207
geneviewrs515726207
scholarrs515726207
googlers515726207
pharmgkbrs515726207
gwascentralrs515726207
openSNPrs515726207
23andMers515726207
23andMe allrs515726207
SNP Nexus

SNPshotrs515726207
SNPdbers515726207
MSV3drs515726207
GWAS Ctlgrs515726207
Max Magnitude0
ClinVar
Risk rs515726207(G;G)
Alt rs515726207(G;G)
Reference rs515726207(A;A)
Significance Pathogenic
Disease Hereditary pancreatitis
Variation info
Gene SPINK1
CLNDBN Hereditary pancreatitis
Reversed 0
HGVS NC_000005.9:g.147207619A>G
CLNSRC ClinVar
CLNACC RCV000119033.2,