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rs587779219

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs587779219(-;-)
Make rs587779219(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799611
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779219
ebirs587779219
HLIrs587779219
Exacrs587779219
Varsomers587779219
Maprs587779219
PheGenIrs587779219
hapmaprs587779219
1000 genomesrs587779219
hgdprs587779219
ensemblrs587779219
gopubmedrs587779219
geneviewrs587779219
scholarrs587779219
googlers587779219
pharmgkbrs587779219
gwascentralrs587779219
openSNPrs587779219
23andMers587779219
23andMe allrs587779219
SNP Nexus

SNPshotrs587779219
SNPdbers587779219
MSV3drs587779219
GWAS Ctlgrs587779219
Max Magnitude0
ClinVar
Risk rs587779219(;)
Alt rs587779219(;)
Reference rs587779219(AA;AA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026750_48026751delAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074672.2,