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rs587778541

From SNPedia

Orientationminus
Geno Mag Summary
(GGA;GGA) 0 common in clinvar
Make rs587778541(-;-)
Make rs587778541(-;GGA)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position45331219
GeneMUTYH
is asnp
is mentioned by
dbSNPrs587778541
ebirs587778541
HLIrs587778541
Exacrs587778541
Varsomers587778541
Maprs587778541
PheGenIrs587778541
hapmaprs587778541
1000 genomesrs587778541
hgdprs587778541
ensemblrs587778541
gopubmedrs587778541
geneviewrs587778541
scholarrs587778541
googlers587778541
pharmgkbrs587778541
gwascentralrs587778541
openSNPrs587778541
23andMers587778541
23andMe allrs587778541
SNP Nexus

SNPshotrs587778541
SNPdbers587778541
MSV3drs587778541
GWAS Ctlgrs587778541
Max Magnitude0
ClinVar
Risk rs587778541(;)
Alt rs587778541(;)
Reference rs587778541(GGA;GGA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified MYH-associated polyposis not provided
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome not specified MYH-associated polyposis not provided
Reversed 1
HGVS NC_000001.10:g.45796891_45796893delTCC
CLNSRC
CLNACC RCV000115758.5, RCV000121599.1, RCV000123145.4, RCV000212719.2,