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rs786204050

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204050(-;-)
Make rs786204050(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47478342
GeneMSH2
is asnp
is mentioned by
dbSNPrs786204050
ebirs786204050
HLIrs786204050
Exacrs786204050
Varsomers786204050
Maprs786204050
PheGenIrs786204050
hapmaprs786204050
1000 genomesrs786204050
hgdprs786204050
ensemblrs786204050
gopubmedrs786204050
geneviewrs786204050
scholarrs786204050
googlers786204050
pharmgkbrs786204050
gwascentralrs786204050
openSNPrs786204050
23andMers786204050
23andMe allrs786204050
SNP Nexus

SNPshotrs786204050
SNPdbers786204050
MSV3drs786204050
GWAS Ctlgrs786204050
Max Magnitude0
ClinVar
Risk rs786204050(;)
Alt rs786204050(;)
Reference rs786204050(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705481delG
CLNSRC
CLNACC RCV000167895.1,