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rs587776618

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776618(-;-)
Make rs587776618(-;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position45331197
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587776618
ebirs587776618
HLIrs587776618
Exacrs587776618
Varsomers587776618
Maprs587776618
PheGenIrs587776618
hapmaprs587776618
1000 genomesrs587776618
hgdprs587776618
ensemblrs587776618
gopubmedrs587776618
geneviewrs587776618
scholarrs587776618
googlers587776618
pharmgkbrs587776618
gwascentralrs587776618
openSNPrs587776618
23andMers587776618
23andMe allrs587776618
SNP Nexus

SNPshotrs587776618
SNPdbers587776618
MSV3drs587776618
GWAS Ctlgrs587776618
Max Magnitude0
ClinVar
Risk rs587776618(GA,A;GA,A)
Alt rs587776618(GA,A;GA,A)
Reference rs587776618(CA;CA)
Significance Pathogenic
Disease MYH-associated polyposis
Variation info
Gene MUTYH
CLNDBN MYH-associated polyposis
Reversed 1
HGVS NC_000001.10:g.45796869delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000005616.2,