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rs515726209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs515726209(A;A)
Make rs515726209(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position15440577
GeneCTRC
is asnp
is mentioned by
dbSNPrs515726209
ebirs515726209
HLIrs515726209
Exacrs515726209
Varsomers515726209
Maprs515726209
PheGenIrs515726209
hapmaprs515726209
1000 genomesrs515726209
hgdprs515726209
ensemblrs515726209
gopubmedrs515726209
geneviewrs515726209
scholarrs515726209
googlers515726209
pharmgkbrs515726209
gwascentralrs515726209
openSNPrs515726209
23andMers515726209
23andMe allrs515726209
SNP Nexus

SNPshotrs515726209
SNPdbers515726209
MSV3drs515726209
GWAS Ctlgrs515726209
Max Magnitude0
ClinVar
Risk rs515726209(A;A)
Alt rs515726209(A;A)
Reference Rs515726209(G;G)
Significance Pathogenic
Disease Hereditary pancreatitis
Variation info
Gene CTRC
CLNDBN Hereditary pancreatitis
Reversed 0
HGVS NC_000001.10:g.15767073G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000119044.2,