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rs121908383

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121908383(A;G)
Make rs121908383(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position45331502
GeneMUTYH
is asnp
is mentioned by
dbSNPrs121908383
ebirs121908383
HLIrs121908383
Exacrs121908383
Varsomers121908383
Maprs121908383
PheGenIrs121908383
hapmaprs121908383
1000 genomesrs121908383
hgdprs121908383
ensemblrs121908383
gopubmedrs121908383
geneviewrs121908383
scholarrs121908383
googlers121908383
pharmgkbrs121908383
gwascentralrs121908383
openSNPrs121908383
23andMers121908383
23andMe allrs121908383
SNP Nexus

SNPshotrs121908383
SNPdbers121908383
MSV3drs121908383
GWAS Ctlgrs121908383
Max Magnitude0
OMIM604933
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121908383(G;G)
Alt rs121908383(G;G)
Reference rs121908383(A;A)
Significance Pathogenic
Disease Neoplasm of stomach
Variation info
Gene MUTYH
CLNDBN Neoplasm of stomach
Reversed 1
HGVS NC_000001.10:g.45797174T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005620.5,