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rs587779287

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCGTACATTATTT;TCGTACATTATTT) 0 common in clinvar
Make rs587779287(-;-)
Make rs587779287(-;GTACATTATTTTC)
Make rs587779287(GTACATTATTTTC;GTACATTATTTTC)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806282
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779287
dbSNP (old)rs587779287
ClinGenrs587779287
ebirs587779287
HLIrs587779287
Exacrs587779287
Gnomadrs587779287
Varsomers587779287
Maprs587779287
PheGenIrs587779287
Biobankrs587779287
1000 genomesrs587779287
hgdprs587779287
ensemblrs587779287
gopubmedrs587779287
geneviewrs587779287
scholarrs587779287
googlers587779287
pharmgkbrs587779287
gwascentralrs587779287
openSNPrs587779287
23andMers587779287
23andMe allrs587779287
SNP Nexus

SNPshotrs587779287
SNPdbers587779287
MSV3drs587779287
GWAS Ctlgrs587779287
Max Magnitude0
ClinVar
Risk rs587779287(-;-)
Alt rs587779287(-;-)
Reference Rs587779287(TCGTACATTATTT;TCGTACATTATTT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033421_48033433delGTACATTATTTTC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074921.2,