Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607915

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607915(-;-)
Make rs267607915(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403211
GeneMSH2
is asnp
is mentioned by
dbSNPrs267607915
ebirs267607915
HLIrs267607915
Exacrs267607915
Varsomers267607915
Maprs267607915
PheGenIrs267607915
hapmaprs267607915
1000 genomesrs267607915
hgdprs267607915
ensemblrs267607915
gopubmedrs267607915
geneviewrs267607915
scholarrs267607915
googlers267607915
pharmgkbrs267607915
gwascentralrs267607915
openSNPrs267607915
23andMers267607915
23andMe allrs267607915
SNP Nexus

SNPshotrs267607915
SNPdbers267607915
MSV3drs267607915
GWAS Ctlgrs267607915
Max Magnitude0
ClinVar
Risk rs267607915(;)
Alt rs267607915(;)
Reference rs267607915(A;A)
Significance Pathogenic
Disease Lynch syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.47630350delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076388.2, RCV000202031.1, RCV000218615.1,