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rs267608122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608122(A;A)
Make rs267608122(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806651
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs267608122
ebirs267608122
HLIrs267608122
Exacrs267608122
Varsomers267608122
Maprs267608122
PheGenIrs267608122
hapmaprs267608122
1000 genomesrs267608122
hgdprs267608122
ensemblrs267608122
gopubmedrs267608122
geneviewrs267608122
scholarrs267608122
googlers267608122
pharmgkbrs267608122
gwascentralrs267608122
openSNPrs267608122
23andMers267608122
23andMe allrs267608122
SNP Nexus

SNPshotrs267608122
SNPdbers267608122
MSV3drs267608122
GWAS Ctlgrs267608122
Max Magnitude0
ClinVar
Risk rs267608122(A;A)
Alt rs267608122(A;A)
Reference rs267608122(G;G)
Significance Pathogenic
Disease Lynch syndrome not provided not specified Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome not provided not specified Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48033790G>A; NC_000002.11:g.48033790G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074974.2, RCV000160701.2, RCV000202090.1, RCV000219938.1,