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rs786203213

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203213(-;-)
Make rs786203213(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position45333315
GeneMUTYH
is asnp
is mentioned by
dbSNPrs786203213
ebirs786203213
HLIrs786203213
Exacrs786203213
Varsomers786203213
Maprs786203213
PheGenIrs786203213
hapmaprs786203213
1000 genomesrs786203213
hgdprs786203213
ensemblrs786203213
gopubmedrs786203213
geneviewrs786203213
scholarrs786203213
googlers786203213
pharmgkbrs786203213
gwascentralrs786203213
openSNPrs786203213
23andMers786203213
23andMe allrs786203213
SNP Nexus

SNPshotrs786203213
SNPdbers786203213
MSV3drs786203213
GWAS Ctlgrs786203213
Max Magnitude0
ClinVar
Risk rs786203213(;)
Alt rs786203213(;)
Reference rs786203213(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.45798987delC
CLNSRC
CLNACC RCV000166426.1,