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rs121909294

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909294(A;A)
Make rs121909294(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position15440524
GeneCTRC
is asnp
is mentioned by
dbSNPrs121909294
dbSNP (old)rs121909294
ClinGenrs121909294
ebirs121909294
HLIrs121909294
Exacrs121909294
Gnomadrs121909294
Varsomers121909294
Maprs121909294
PheGenIrs121909294
Biobankrs121909294
1000 genomesrs121909294
hgdprs121909294
ensemblrs121909294
gopubmedrs121909294
geneviewrs121909294
scholarrs121909294
googlers121909294
pharmgkbrs121909294
gwascentralrs121909294
openSNPrs121909294
23andMers121909294
23andMe allrs121909294
SNP Nexus

SNPshotrs121909294
SNPdbers121909294
MSV3drs121909294
GWAS Ctlgrs121909294
Max Magnitude0
OMIM601405
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909294(A;A) rs121909294(T;T)
Alt rs121909294(A;A) rs121909294(T;T)
Reference Rs121909294(G;G)
Significance Other
Disease Pancreatitis Hereditary pancreatitis
Variation info
Gene CTRC
CLNDBN Pancreatitis, chronic, susceptibility to Hereditary pancreatitis
Reversed 0
HGVS NC_000001.10:g.15767020G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008659.2, RCV000119047.2,