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rs267608041

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267608041(-;-)
Make rs267608041(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47798724
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608041
ebirs267608041
HLIrs267608041
Exacrs267608041
Varsomers267608041
Maprs267608041
PheGenIrs267608041
hapmaprs267608041
1000 genomesrs267608041
hgdprs267608041
ensemblrs267608041
gopubmedrs267608041
geneviewrs267608041
scholarrs267608041
googlers267608041
pharmgkbrs267608041
gwascentralrs267608041
openSNPrs267608041
23andMers267608041
23andMe allrs267608041
SNP Nexus

SNPshotrs267608041
SNPdbers267608041
MSV3drs267608041
GWAS Ctlgrs267608041
Max Magnitude0
ClinVar
Risk rs267608041(;)
Alt rs267608041(;)
Reference rs267608041(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025863delA
CLNSRC
CLNACC RCV000231668.1,