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rs864622041

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864622041(C;C)
Make rs864622041(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47805693
GeneMSH6
is asnp
is mentioned by
dbSNPrs864622041
ebirs864622041
HLIrs864622041
Exacrs864622041
Varsomers864622041
Maprs864622041
PheGenIrs864622041
hapmaprs864622041
1000 genomesrs864622041
hgdprs864622041
ensemblrs864622041
gopubmedrs864622041
geneviewrs864622041
scholarrs864622041
googlers864622041
pharmgkbrs864622041
gwascentralrs864622041
openSNPrs864622041
23andMers864622041
23andMe allrs864622041
SNP Nexus

SNPshotrs864622041
SNPdbers864622041
MSV3drs864622041
GWAS Ctlgrs864622041
Max Magnitude0
ClinVar
Risk rs864622041(C;C)
Alt rs864622041(C;C)
Reference rs864622041(T;T)
Significance Pathogenic
Disease Lynch syndrome I Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN Lynch syndrome I Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48032832T>C
CLNSRC
CLNACC RCV000206750.1, RCV000215362.1,