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rs747993448

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747993448(A;A)
Make rs747993448(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45332795
GeneMUTYH
is asnp
is mentioned by
dbSNPrs747993448
ebirs747993448
HLIrs747993448
Exacrs747993448
Varsomers747993448
Maprs747993448
PheGenIrs747993448
hapmaprs747993448
1000 genomesrs747993448
hgdprs747993448
ensemblrs747993448
gopubmedrs747993448
geneviewrs747993448
scholarrs747993448
googlers747993448
pharmgkbrs747993448
gwascentralrs747993448
openSNPrs747993448
23andMers747993448
23andMe allrs747993448
SNP Nexus

SNPshotrs747993448
SNPdbers747993448
MSV3drs747993448
GWAS Ctlgrs747993448
Max Magnitude0
ClinVar
Risk rs747993448(A;A)
Alt rs747993448(A;A)
Reference rs747993448(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome MYH-associated polyposis not provided
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome MYH-associated polyposis not provided
Reversed 0
HGVS NC_000001.10:g.45798467G>A
CLNSRC
CLNACC RCV000166998.1, RCV000229525.1, RCV000236750.1,