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rs587781372

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781372(C;T)
Make rs587781372(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800915
GeneMSH6
is asnp
is mentioned by
dbSNPrs587781372
ebirs587781372
HLIrs587781372
Exacrs587781372
Varsomers587781372
Maprs587781372
PheGenIrs587781372
hapmaprs587781372
1000 genomesrs587781372
hgdprs587781372
ensemblrs587781372
gopubmedrs587781372
geneviewrs587781372
scholarrs587781372
googlers587781372
pharmgkbrs587781372
gwascentralrs587781372
openSNPrs587781372
23andMers587781372
23andMe allrs587781372
SNP Nexus

SNPshotrs587781372
SNPdbers587781372
MSV3drs587781372
GWAS Ctlgrs587781372
Max Magnitude0
ClinVar
Risk rs587781372(G,T;G,T)
Alt rs587781372(G,T;G,T)
Reference rs587781372(C;C)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48028054C>G; NC_000002.11:g.48028054C>T
CLNSRC
CLNACC RCV000229215.1, RCV000129185.2, RCV000202022.1,