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rs376561094

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376561094(A;A)
Make rs376561094(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45332636
GeneMUTYH
is asnp
is mentioned by
dbSNPrs376561094
ebirs376561094
HLIrs376561094
Exacrs376561094
Varsomers376561094
Maprs376561094
PheGenIrs376561094
hapmaprs376561094
1000 genomesrs376561094
hgdprs376561094
ensemblrs376561094
gopubmedrs376561094
geneviewrs376561094
scholarrs376561094
googlers376561094
pharmgkbrs376561094
gwascentralrs376561094
openSNPrs376561094
23andMers376561094
23andMe allrs376561094
SNP Nexus

SNPshotrs376561094
SNPdbers376561094
MSV3drs376561094
GWAS Ctlgrs376561094
Max Magnitude0
ClinVar
Risk rs376561094(A;A)
Alt rs376561094(A;A)
Reference rs376561094(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MUTYH
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000001.10:g.45798308G>A
CLNSRC
CLNACC RCV000223123.1,