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rs587779174

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779174(-;-)
Make rs587779174(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47412459
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779174
ebirs587779174
HLIrs587779174
Exacrs587779174
Varsomers587779174
Maprs587779174
PheGenIrs587779174
hapmaprs587779174
1000 genomesrs587779174
hgdprs587779174
ensemblrs587779174
gopubmedrs587779174
geneviewrs587779174
scholarrs587779174
googlers587779174
pharmgkbrs587779174
gwascentralrs587779174
openSNPrs587779174
23andMers587779174
23andMe allrs587779174
SNP Nexus

SNPshotrs587779174
SNPdbers587779174
MSV3drs587779174
GWAS Ctlgrs587779174
Max Magnitude0
ClinVar
Risk rs587779174(;)
Alt rs587779174(;)
Reference rs587779174(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639598delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076683.2,