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rs876659414

From SNPedia

Orientationminus
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
ebirs876659414
HLIrs876659414
Exacrs876659414
Varsomers876659414
Maprs876659414
PheGenIrs876659414
hapmaprs876659414
1000 genomesrs876659414
hgdprs876659414
ensemblrs876659414
gopubmedrs876659414
geneviewrs876659414
scholarrs876659414
googlers876659414
pharmgkbrs876659414
gwascentralrs876659414
openSNPrs876659414
23andMers876659414
23andMe allrs876659414
SNP Nexus

SNPshotrs876659414
SNPdbers876659414
MSV3drs876659414
GWAS Ctlgrs876659414
Max Magnitude0
ClinVar
Risk rs876659414(;)
Alt rs876659414(;)
Reference rs876659414(TC;TC)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MUTYH
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.45796988_45796989delGA
CLNSRC
CLNACC RCV000217438.1,