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rs864622121

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs864622121(-;-)
Make rs864622121(-;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47475228
GeneMSH2
is asnp
is mentioned by
dbSNPrs864622121
dbSNP (old)rs864622121
ClinGenrs864622121
ebirs864622121
HLIrs864622121
Exacrs864622121
Gnomadrs864622121
Varsomers864622121
Maprs864622121
PheGenIrs864622121
Biobankrs864622121
1000 genomesrs864622121
hgdprs864622121
ensemblrs864622121
gopubmedrs864622121
geneviewrs864622121
scholarrs864622121
googlers864622121
pharmgkbrs864622121
gwascentralrs864622121
openSNPrs864622121
23andMers864622121
23andMe allrs864622121
SNP Nexus

SNPshotrs864622121
SNPdbers864622121
MSV3drs864622121
GWAS Ctlgrs864622121
Max Magnitude0
ClinVar
Risk rs864622121(-;-)
Alt rs864622121(-;-)
Reference Rs864622121(GT;GT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702367_47702368delGT
CLNSRC
CLNACC RCV000204789.1,