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rs864622340

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864622340(-;-)
Make rs864622340(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47416376
GeneMSH2
is asnp
is mentioned by
dbSNPrs864622340
dbSNP (old)rs864622340
ClinGenrs864622340
ebirs864622340
HLIrs864622340
Exacrs864622340
Gnomadrs864622340
Varsomers864622340
Maprs864622340
PheGenIrs864622340
Biobankrs864622340
1000 genomesrs864622340
hgdprs864622340
ensemblrs864622340
gopubmedrs864622340
geneviewrs864622340
scholarrs864622340
googlers864622340
pharmgkbrs864622340
gwascentralrs864622340
openSNPrs864622340
23andMers864622340
23andMe allrs864622340
SNP Nexus

SNPshotrs864622340
SNPdbers864622340
MSV3drs864622340
GWAS Ctlgrs864622340
Max Magnitude0
ClinVar
Risk rs864622340(-;-)
Alt rs864622340(-;-)
Reference Rs864622340(T;T)
Significance Pathogenic
Disease Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47643515delT
CLNSRC
CLNACC RCV000206764.1, RCV000478573.1, RCV000491587.1,