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rs786205215

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205215(C;T)
Make rs786205215(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position58363582
GeneRNF43
is asnp
is mentioned by
dbSNPrs786205215
ebirs786205215
HLIrs786205215
Exacrs786205215
Varsomers786205215
Maprs786205215
PheGenIrs786205215
hapmaprs786205215
1000 genomesrs786205215
hgdprs786205215
ensemblrs786205215
gopubmedrs786205215
geneviewrs786205215
scholarrs786205215
googlers786205215
pharmgkbrs786205215
gwascentralrs786205215
openSNPrs786205215
23andMers786205215
23andMe allrs786205215
SNP Nexus

SNPshotrs786205215
SNPdbers786205215
MSV3drs786205215
GWAS Ctlgrs786205215
Max Magnitude0
ClinVar
Risk rs786205215(T;T)
Alt rs786205215(T;T)
Reference rs786205215(C;C)
Significance Pathogenic
Disease Colon Serrated Polyposis
Variation info
Gene RNF43
CLNDBN Colon Serrated Polyposis
Reversed 1
HGVS NC_000017.10:g.56440943G>A
CLNSRC
CLNACC RCV000170445.1,