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rs876659420

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659420(G;T)
Make rs876659420(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45330515
GeneMUTYH
is asnp
is mentioned by
dbSNPrs876659420
ebirs876659420
HLIrs876659420
Exacrs876659420
Varsomers876659420
Maprs876659420
PheGenIrs876659420
hapmaprs876659420
1000 genomesrs876659420
hgdprs876659420
ensemblrs876659420
gopubmedrs876659420
geneviewrs876659420
scholarrs876659420
googlers876659420
pharmgkbrs876659420
gwascentralrs876659420
openSNPrs876659420
23andMers876659420
23andMe allrs876659420
SNP Nexus

SNPshotrs876659420
SNPdbers876659420
MSV3drs876659420
GWAS Ctlgrs876659420
Max Magnitude0
ClinVar
Risk rs876659420(T;T)
Alt rs876659420(T;T)
Reference rs876659420(G;G)
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.45796187C>A
CLNSRC
CLNACC RCV000223520.1,