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rs869312769

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312769(-;-)
Make rs869312769(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47799335
GeneMSH6
is asnp
is mentioned by
dbSNPrs869312769
ebirs869312769
HLIrs869312769
Exacrs869312769
Varsomers869312769
Maprs869312769
PheGenIrs869312769
hapmaprs869312769
1000 genomesrs869312769
hgdprs869312769
ensemblrs869312769
gopubmedrs869312769
geneviewrs869312769
scholarrs869312769
googlers869312769
pharmgkbrs869312769
gwascentralrs869312769
openSNPrs869312769
23andMers869312769
23andMe allrs869312769
SNP Nexus

SNPshotrs869312769
SNPdbers869312769
MSV3drs869312769
GWAS Ctlgrs869312769
Max Magnitude0
ClinVar
Risk rs869312769(;)
Alt rs869312769(;)
Reference rs869312769(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026474delT
CLNSRC
CLNACC RCV000210100.1,