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rs587779221

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779221(-;-)
Make rs587779221(-;A)
Make rs587779221(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799802
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779221
ebirs587779221
HLIrs587779221
Exacrs587779221
Varsomers587779221
Maprs587779221
PheGenIrs587779221
hapmaprs587779221
1000 genomesrs587779221
hgdprs587779221
ensemblrs587779221
gopubmedrs587779221
geneviewrs587779221
scholarrs587779221
googlers587779221
pharmgkbrs587779221
gwascentralrs587779221
openSNPrs587779221
23andMers587779221
23andMe allrs587779221
SNP Nexus

SNPshotrs587779221
SNPdbers587779221
MSV3drs587779221
GWAS Ctlgrs587779221
Max Magnitude0
ClinVar
Risk rs587779221(A;A)
Alt rs587779221(A;A)
Reference rs587779221(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026941dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074688.2,