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rs876660190

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660190(-;-)
Make rs876660190(-;ATGGAT)
Make rs876660190(ATGGAT;ATGGAT)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45333100
GeneMUTYH
is asnp
is mentioned by
dbSNPrs876660190
ebirs876660190
HLIrs876660190
Exacrs876660190
Varsomers876660190
Maprs876660190
PheGenIrs876660190
hapmaprs876660190
1000 genomesrs876660190
hgdprs876660190
ensemblrs876660190
gopubmedrs876660190
geneviewrs876660190
scholarrs876660190
googlers876660190
pharmgkbrs876660190
gwascentralrs876660190
openSNPrs876660190
23andMers876660190
23andMe allrs876660190
SNP Nexus

SNPshotrs876660190
SNPdbers876660190
MSV3drs876660190
GWAS Ctlgrs876660190
Max Magnitude0
ClinVar
Risk rs876660190(ATGGAT;ATGGAT)
Alt rs876660190(ATGGAT;ATGGAT)
Reference rs876660190(;)
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.45798773_45798778dupATCCAT
CLNSRC
CLNACC RCV000215777.1,