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rs864622183

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622183(G;T)
Make rs864622183(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47412516
GeneMSH2
is asnp
is mentioned by
dbSNPrs864622183
ebirs864622183
HLIrs864622183
Exacrs864622183
Varsomers864622183
Maprs864622183
PheGenIrs864622183
hapmaprs864622183
1000 genomesrs864622183
hgdprs864622183
ensemblrs864622183
gopubmedrs864622183
geneviewrs864622183
scholarrs864622183
googlers864622183
pharmgkbrs864622183
gwascentralrs864622183
openSNPrs864622183
23andMers864622183
23andMe allrs864622183
SNP Nexus

SNPshotrs864622183
SNPdbers864622183
MSV3drs864622183
GWAS Ctlgrs864622183
Max Magnitude0
ClinVar
Risk rs864622183(T;T)
Alt rs864622183(T;T)
Reference rs864622183(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639655G>T
CLNSRC
CLNACC RCV000204356.1,