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rs587782712

From SNPedia

Orientationplus
Geno Mag Summary
(GAAAA;GAAAA) 0 common in clinvar
Make rs587782712(-;-)
Make rs587782712(-;AAGAA)
Make rs587782712(AAGAA;AAGAA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47801020
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782712
ebirs587782712
HLIrs587782712
Exacrs587782712
Varsomers587782712
Maprs587782712
PheGenIrs587782712
hapmaprs587782712
1000 genomesrs587782712
hgdprs587782712
ensemblrs587782712
gopubmedrs587782712
geneviewrs587782712
scholarrs587782712
googlers587782712
pharmgkbrs587782712
gwascentralrs587782712
openSNPrs587782712
23andMers587782712
23andMe allrs587782712
SNP Nexus

SNPshotrs587782712
SNPdbers587782712
MSV3drs587782712
GWAS Ctlgrs587782712
Max Magnitude0
ClinVar
Risk rs587782712(;)
Alt rs587782712(;)
Reference rs587782712(GAAAA;GAAAA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48028159_48028163delAAGAA
CLNSRC
CLNACC RCV000132188.2, RCV000200490.1, RCV000202303.1,