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rs786204144

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204144(-;-)
Make rs786204144(-;A)
Make rs786204144(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47412550
GeneMSH2
is asnp
is mentioned by
dbSNPrs786204144
ebirs786204144
HLIrs786204144
Exacrs786204144
Varsomers786204144
Maprs786204144
PheGenIrs786204144
hapmaprs786204144
1000 genomesrs786204144
hgdprs786204144
ensemblrs786204144
gopubmedrs786204144
geneviewrs786204144
scholarrs786204144
googlers786204144
pharmgkbrs786204144
gwascentralrs786204144
openSNPrs786204144
23andMers786204144
23andMe allrs786204144
SNP Nexus

SNPshotrs786204144
SNPdbers786204144
MSV3drs786204144
GWAS Ctlgrs786204144
Max Magnitude0
ClinVar
Risk rs786204144(A;A)
Alt rs786204144(A;A)
Reference rs786204144(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639689_47639690insA
CLNSRC
CLNACC RCV000168130.1,