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rs876659625

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659625(C;T)
Make rs876659625(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45333138
GeneMUTYH
is asnp
is mentioned by
dbSNPrs876659625
ebirs876659625
HLIrs876659625
Exacrs876659625
Varsomers876659625
Maprs876659625
PheGenIrs876659625
hapmaprs876659625
1000 genomesrs876659625
hgdprs876659625
ensemblrs876659625
gopubmedrs876659625
geneviewrs876659625
scholarrs876659625
googlers876659625
pharmgkbrs876659625
gwascentralrs876659625
openSNPrs876659625
23andMers876659625
23andMe allrs876659625
SNP Nexus

SNPshotrs876659625
SNPdbers876659625
MSV3drs876659625
GWAS Ctlgrs876659625
Max Magnitude0
ClinVar
Risk rs876659625(T;T)
Alt rs876659625(T;T)
Reference rs876659625(C;C)
Significance 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.45798810G>A
CLNSRC
CLNACC RCV000219018.1,