Have questions? Visit https://www.reddit.com/r/SNPedia

rs773087549

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773087549(A;A)
Make rs773087549(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45332401
GeneMUTYH
is asnp
is mentioned by
dbSNPrs773087549
ebirs773087549
HLIrs773087549
Exacrs773087549
Varsomers773087549
Maprs773087549
PheGenIrs773087549
hapmaprs773087549
1000 genomesrs773087549
hgdprs773087549
ensemblrs773087549
gopubmedrs773087549
geneviewrs773087549
scholarrs773087549
googlers773087549
pharmgkbrs773087549
gwascentralrs773087549
openSNPrs773087549
23andMers773087549
23andMe allrs773087549
SNP Nexus

SNPshotrs773087549
SNPdbers773087549
MSV3drs773087549
GWAS Ctlgrs773087549
Max Magnitude0
ClinVar
Risk rs773087549(A;A)
Alt rs773087549(A;A)
Reference rs773087549(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MUTYH
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.45798073G>A
CLNSRC
CLNACC RCV000235928.1,