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rs587780670

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587780670(-;-)
Make rs587780670(-;A)
Make rs587780670(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799773
GeneMSH6
is asnp
is mentioned by
dbSNPrs587780670
ebirs587780670
HLIrs587780670
Exacrs587780670
Varsomers587780670
Maprs587780670
PheGenIrs587780670
hapmaprs587780670
1000 genomesrs587780670
hgdprs587780670
ensemblrs587780670
gopubmedrs587780670
geneviewrs587780670
scholarrs587780670
googlers587780670
pharmgkbrs587780670
gwascentralrs587780670
openSNPrs587780670
23andMers587780670
23andMe allrs587780670
SNP Nexus

SNPshotrs587780670
SNPdbers587780670
MSV3drs587780670
GWAS Ctlgrs587780670
Max Magnitude0
ClinVar
Risk rs587780670(A;A)
Alt rs587780670(A;A)
Reference rs587780670(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026912dupA
CLNSRC
CLNACC RCV000122953.1,