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rs267608064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAA;AAAA) 0 common in clinvar
Make rs267608064(-;-)
Make rs267608064(-;AAAA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799615
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608064
ebirs267608064
HLIrs267608064
Exacrs267608064
Varsomers267608064
Maprs267608064
PheGenIrs267608064
hapmaprs267608064
1000 genomesrs267608064
hgdprs267608064
ensemblrs267608064
gopubmedrs267608064
geneviewrs267608064
scholarrs267608064
googlers267608064
pharmgkbrs267608064
gwascentralrs267608064
openSNPrs267608064
23andMers267608064
23andMe allrs267608064
SNP Nexus

SNPshotrs267608064
SNPdbers267608064
MSV3drs267608064
GWAS Ctlgrs267608064
Max Magnitude0
ClinVar
Risk rs267608064(;)
Alt rs267608064(;)
Reference rs267608064(AAAA;AAAA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026754_48026757delAAAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074673.2,