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rs587779102

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779102(G;T)
Make rs587779102(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47403357
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779102
ebirs587779102
HLIrs587779102
Exacrs587779102
Varsomers587779102
Maprs587779102
PheGenIrs587779102
hapmaprs587779102
1000 genomesrs587779102
hgdprs587779102
ensemblrs587779102
gopubmedrs587779102
geneviewrs587779102
scholarrs587779102
googlers587779102
pharmgkbrs587779102
gwascentralrs587779102
openSNPrs587779102
23andMers587779102
23andMe allrs587779102
SNP Nexus

SNPshotrs587779102
SNPdbers587779102
MSV3drs587779102
GWAS Ctlgrs587779102
Max Magnitude0
ClinVar
Risk rs587779102(A,T;A,T)
Alt rs587779102(A,T;A,T)
Reference rs587779102(G;G)
Significance Pathogenic
Disease Lynch syndrome not specified
Variation info
Gene MSH2
CLNDBN Lynch syndrome not specified
Reversed 0
HGVS NC_000002.11:g.47630496G>A; NC_000002.11:g.47630496G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000122982.1, RCV000235661.1, RCV000076238.2,