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rs587779206

From SNPedia

Orientationplus
Geno Mag Summary
(GAGAT;GAGAT) 0 common in clinvar
Make rs587779206(-;-)
Make rs587779206(-;ATGAG)
Make rs587779206(ATGAG;ATGAG)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799122
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779206
ebirs587779206
HLIrs587779206
Exacrs587779206
Varsomers587779206
Maprs587779206
PheGenIrs587779206
hapmaprs587779206
1000 genomesrs587779206
hgdprs587779206
ensemblrs587779206
gopubmedrs587779206
geneviewrs587779206
scholarrs587779206
googlers587779206
pharmgkbrs587779206
gwascentralrs587779206
openSNPrs587779206
23andMers587779206
23andMe allrs587779206
SNP Nexus

SNPshotrs587779206
SNPdbers587779206
MSV3drs587779206
GWAS Ctlgrs587779206
Max Magnitude0
ClinVar
Risk rs587779206(;)
Alt rs587779206(;)
Reference rs587779206(GAGAT;GAGAT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026261_48026265delATGAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074636.2,