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rs267608035

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608035(A;A)
Make rs267608035(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47795893
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608035
ebirs267608035
HLIrs267608035
Exacrs267608035
Varsomers267608035
Maprs267608035
PheGenIrs267608035
hapmaprs267608035
1000 genomesrs267608035
hgdprs267608035
ensemblrs267608035
gopubmedrs267608035
geneviewrs267608035
scholarrs267608035
googlers267608035
pharmgkbrs267608035
gwascentralrs267608035
openSNPrs267608035
23andMers267608035
23andMe allrs267608035
SNP Nexus

SNPshotrs267608035
SNPdbers267608035
MSV3drs267608035
GWAS Ctlgrs267608035
Max Magnitude0
ClinVar
Risk rs267608035(A;A)
Alt rs267608035(A;A)
Reference rs267608035(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48023032G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075000.2,