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rs587779100

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779100(-;-)
Make rs587779100(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47470970
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779100
ebirs587779100
HLIrs587779100
Exacrs587779100
Varsomers587779100
Maprs587779100
PheGenIrs587779100
hapmaprs587779100
1000 genomesrs587779100
hgdprs587779100
ensemblrs587779100
gopubmedrs587779100
geneviewrs587779100
scholarrs587779100
googlers587779100
pharmgkbrs587779100
gwascentralrs587779100
openSNPrs587779100
23andMers587779100
23andMe allrs587779100
SNP Nexus

SNPshotrs587779100
SNPdbers587779100
MSV3drs587779100
GWAS Ctlgrs587779100
Max Magnitude0
ClinVar
Risk rs587779100(;)
Alt rs587779100(;)
Reference rs587779100(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698109delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076236.2,