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rs281864945

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281864945(-;-)
Make rs281864945(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412473
GeneMSH2
is asnp
is mentioned by
dbSNPrs281864945
ebirs281864945
HLIrs281864945
Exacrs281864945
Varsomers281864945
Maprs281864945
PheGenIrs281864945
hapmaprs281864945
1000 genomesrs281864945
hgdprs281864945
ensemblrs281864945
gopubmedrs281864945
geneviewrs281864945
scholarrs281864945
googlers281864945
pharmgkbrs281864945
gwascentralrs281864945
openSNPrs281864945
23andMers281864945
23andMe allrs281864945
SNP Nexus

SNPshotrs281864945
SNPdbers281864945
MSV3drs281864945
GWAS Ctlgrs281864945
Max Magnitude0
ClinVar
Risk rs281864945(;)
Alt rs281864945(;)
Reference rs281864945(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639612delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076687.2,