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rs121909293

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909293(C;T)
Make rs121909293(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position15445717
GeneCTRC
is asnp
is mentioned by
dbSNPrs121909293
ebirs121909293
HLIrs121909293
Exacrs121909293
Varsomers121909293
Maprs121909293
PheGenIrs121909293
hapmaprs121909293
1000 genomesrs121909293
hgdprs121909293
ensemblrs121909293
gopubmedrs121909293
geneviewrs121909293
scholarrs121909293
googlers121909293
pharmgkbrs121909293
gwascentralrs121909293
openSNPrs121909293
23andMers121909293
23andMe allrs121909293
SNP Nexus

SNPshotrs121909293
SNPdbers121909293
MSV3drs121909293
GWAS Ctlgrs121909293
GMAF0.004132
Max Magnitude0
OMIM601405
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909293(T;T)
Alt rs121909293(T;T)
Reference rs121909293(C;C)
Significance Other
Disease Pancreatitis Hereditary pancreatitis
Variation info
Gene CTRC
CLNDBN Pancreatitis, chronic, susceptibility to Hereditary pancreatitis
Reversed 0
HGVS NC_000001.10:g.15772212C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008657.2, RCV000119045.2,