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rs587779936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs587779936(-;ACCA)
Make rs587779936(ACCA;ACCA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806306
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779936
dbSNP (old)rs587779936
ClinGenrs587779936
ebirs587779936
HLIrs587779936
Exacrs587779936
Gnomadrs587779936
Varsomers587779936
Maprs587779936
PheGenIrs587779936
Biobankrs587779936
1000 genomesrs587779936
hgdprs587779936
ensemblrs587779936
gopubmedrs587779936
geneviewrs587779936
scholarrs587779936
googlers587779936
pharmgkbrs587779936
gwascentralrs587779936
openSNPrs587779936
23andMers587779936
23andMe allrs587779936
SNP Nexus

SNPshotrs587779936
SNPdbers587779936
MSV3drs587779936
GWAS Ctlgrs587779936
Max Magnitude0
ClinVar
Risk rs587779936(ACCA;ACCA)
Alt rs587779936(ACCA;ACCA)
Reference Rs587779936(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48033442_48033445dupACCA
CLNSRC
CLNACC RCV000115420.2,