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rs730881833

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881833(A;A)
Make rs730881833(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45332242
GeneMUTYH
is asnp
is mentioned by
dbSNPrs730881833
ebirs730881833
HLIrs730881833
Exacrs730881833
Varsomers730881833
Maprs730881833
PheGenIrs730881833
hapmaprs730881833
1000 genomesrs730881833
hgdprs730881833
ensemblrs730881833
gopubmedrs730881833
geneviewrs730881833
scholarrs730881833
googlers730881833
pharmgkbrs730881833
gwascentralrs730881833
openSNPrs730881833
23andMers730881833
23andMe allrs730881833
SNP Nexus

SNPshotrs730881833
SNPdbers730881833
MSV3drs730881833
GWAS Ctlgrs730881833
Max Magnitude0
ClinVar
Risk rs730881833(A,T;A,T)
Alt rs730881833(A,T;A,T)
Reference rs730881833(G;G)
Significance Pathogenic
Disease not provided MYH-associated polyposis Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MUTYH
CLNDBN not provided MYH-associated polyposis Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.45797914C>T
CLNSRC
CLNACC RCV000160754.2, RCV000191933.1, RCV000221854.1,