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rs876659414

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs876659414(-;-)
Make rs876659414(-;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45331316
GeneMUTYH
is asnp
is mentioned by
dbSNPrs876659414
dbSNP (classic)rs876659414
ClinGenrs876659414
ebirs876659414
HLIrs876659414
Exacrs876659414
Gnomadrs876659414
Varsomers876659414
LitVarrs876659414
Maprs876659414
PheGenIrs876659414
Biobankrs876659414
1000 genomesrs876659414
hgdprs876659414
ensemblrs876659414
geneviewrs876659414
scholarrs876659414
googlers876659414
pharmgkbrs876659414
gwascentralrs876659414
openSNPrs876659414
23andMers876659414
SNPshotrs876659414
SNPdbers876659414
MSV3drs876659414
GWAS Ctlgrs876659414
Max Magnitude0
ClinVar
Risk rs876659414(-;-)
Alt rs876659414(-;-)
Reference Rs876659414(TC;TC)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MUTYH
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.45796988_45796989delGA
CLNSRC
CLNACC RCV000217438.1,