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rs587779194

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779194(-;-)
Make rs587779194(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47414420
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779194
ClinGenrs587779194
ebirs587779194
HLIrs587779194
Exacrs587779194
Varsomers587779194
Maprs587779194
PheGenIrs587779194
hapmaprs587779194
1000 genomesrs587779194
hgdprs587779194
ensemblrs587779194
gopubmedrs587779194
geneviewrs587779194
scholarrs587779194
googlers587779194
pharmgkbrs587779194
gwascentralrs587779194
openSNPrs587779194
23andMers587779194
23andMe allrs587779194
SNP Nexus

SNPshotrs587779194
SNPdbers587779194
MSV3drs587779194
GWAS Ctlgrs587779194
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs587779194(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641559delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076755.2,