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rs587779218

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs587779218(G;G)
Make rs587779218(G;TC)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799597
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779218
ebirs587779218
HLIrs587779218
Exacrs587779218
Varsomers587779218
Maprs587779218
PheGenIrs587779218
hapmaprs587779218
1000 genomesrs587779218
hgdprs587779218
ensemblrs587779218
gopubmedrs587779218
geneviewrs587779218
scholarrs587779218
googlers587779218
pharmgkbrs587779218
gwascentralrs587779218
openSNPrs587779218
23andMers587779218
23andMe allrs587779218
SNP Nexus

SNPshotrs587779218
SNPdbers587779218
MSV3drs587779218
GWAS Ctlgrs587779218
Max Magnitude0
ClinVar
Risk rs587779218(G;G)
Alt rs587779218(G;G)
Reference rs587779218(TC;TC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026736_48026737delTCinsG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074670.2,