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rs763673818

From SNPedia

Merged intors63750767
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs763673818(-;TCAAAAGGGACATAGAAAA)
Make rs763673818(TCAAAAGGGACATAGAAAA;TCAAAAGGGACATAGAAAA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47806588
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs763673818
dbSNP (old)rs763673818
ClinGenrs763673818
ebirs763673818
HLIrs763673818
Exacrs763673818
Varsomers763673818
Maprs763673818
PheGenIrs763673818
Biobankrs763673818
1000 genomesrs763673818
hgdprs763673818
ensemblrs763673818
gopubmedrs763673818
geneviewrs763673818
scholarrs763673818
googlers763673818
pharmgkbrs763673818
gwascentralrs763673818
openSNPrs763673818
23andMers763673818
23andMe allrs763673818
SNP Nexus

SNPshotrs763673818
SNPdbers763673818
MSV3drs763673818
GWAS Ctlgrs763673818
StatusMerged into rs63750767
Max Magnitude0
ClinVar
Risk rs763673818(TCAAAAGGGACATAGAAAA;TCAAAAGGGACATAGAAAA)
Alt rs763673818(TCAAAAGGGACATAGAAAA;TCAAAAGGGACATAGAAAA)
Reference Rs763673818(;)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48033728_48033746dup19
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074954.2, RCV000129554.5, RCV000202115.1,