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rs587782277

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587782277(-;-)
Make rs587782277(-;A)
Make rs587782277(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800762
GeneMSH6
is asnp
is mentioned by
dbSNPrs587782277
ebirs587782277
HLIrs587782277
Exacrs587782277
Varsomers587782277
Maprs587782277
PheGenIrs587782277
hapmaprs587782277
1000 genomesrs587782277
hgdprs587782277
ensemblrs587782277
gopubmedrs587782277
geneviewrs587782277
scholarrs587782277
googlers587782277
pharmgkbrs587782277
gwascentralrs587782277
openSNPrs587782277
23andMers587782277
23andMe allrs587782277
SNP Nexus

SNPshotrs587782277
SNPdbers587782277
MSV3drs587782277
GWAS Ctlgrs587782277
Max Magnitude0
ClinVar
Risk rs587782277(A;A)
Alt rs587782277(A;A)
Reference rs587782277(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48027901dupA
CLNSRC
CLNACC RCV000131134.2, RCV000218611.1,