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rs762307622

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs762307622(C;T)
Make rs762307622(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position45332955
GeneMUTYH
is asnp
is mentioned by
dbSNPrs762307622
ebirs762307622
HLIrs762307622
Exacrs762307622
Varsomers762307622
Maprs762307622
PheGenIrs762307622
hapmaprs762307622
1000 genomesrs762307622
hgdprs762307622
ensemblrs762307622
gopubmedrs762307622
geneviewrs762307622
scholarrs762307622
googlers762307622
pharmgkbrs762307622
gwascentralrs762307622
openSNPrs762307622
23andMers762307622
23andMe allrs762307622
SNP Nexus

SNPshotrs762307622
SNPdbers762307622
MSV3drs762307622
GWAS Ctlgrs762307622
Max Magnitude0
ClinVar
Risk rs762307622(T;T)
Alt rs762307622(T;T)
Reference rs762307622(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene MUTYH
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000001.10:g.45798627C>T
CLNSRC
CLNACC RCV000213856.1, RCV000235993.1,