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rs864621967

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGCACTA;GGCACTA) 0 common in clinvar
Make rs864621967(-;-)
Make rs864621967(-;GGCACTA)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position45331176
GeneMUTYH
is asnp
is mentioned by
dbSNPrs864621967
ClinGenrs864621967
ebirs864621967
HLIrs864621967
Exacrs864621967
Varsomers864621967
Maprs864621967
PheGenIrs864621967
hapmaprs864621967
1000 genomesrs864621967
hgdprs864621967
ensemblrs864621967
gopubmedrs864621967
geneviewrs864621967
scholarrs864621967
googlers864621967
pharmgkbrs864621967
gwascentralrs864621967
openSNPrs864621967
23andMers864621967
23andMe allrs864621967
SNP Nexus

SNPshotrs864621967
SNPdbers864621967
MSV3drs864621967
GWAS Ctlgrs864621967
Max Magnitude0
ClinVar
Risk rs864621967(-;-)
Alt rs864621967(-;-)
Reference Rs864621967(GGCACTA;GGCACTA)
Significance Probable-Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.45796848_45796854delTAGTGCC
CLNSRC
CLNACC RCV000160747.3, RCV000215481.1,