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rs587780538

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780538(A;A)
Make rs587780538(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799350
GeneMSH6
is asnp
is mentioned by
dbSNPrs587780538
ebirs587780538
HLIrs587780538
Exacrs587780538
Varsomers587780538
Maprs587780538
PheGenIrs587780538
hapmaprs587780538
1000 genomesrs587780538
hgdprs587780538
ensemblrs587780538
gopubmedrs587780538
geneviewrs587780538
scholarrs587780538
googlers587780538
pharmgkbrs587780538
gwascentralrs587780538
openSNPrs587780538
23andMers587780538
23andMe allrs587780538
SNP Nexus

SNPshotrs587780538
SNPdbers587780538
MSV3drs587780538
GWAS Ctlgrs587780538
Max Magnitude0
ClinVar
Risk rs587780538(A;A)
Alt rs587780538(A;A)
Reference rs587780538(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026489G>A
CLNSRC
CLNACC RCV000119152.1,