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rs587779234

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779234(A;A)
Make rs587779234(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800313
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779234
ebirs587779234
HLIrs587779234
Exacrs587779234
Varsomers587779234
Maprs587779234
PheGenIrs587779234
hapmaprs587779234
1000 genomesrs587779234
hgdprs587779234
ensemblrs587779234
gopubmedrs587779234
geneviewrs587779234
scholarrs587779234
googlers587779234
pharmgkbrs587779234
gwascentralrs587779234
openSNPrs587779234
23andMers587779234
23andMe allrs587779234
SNP Nexus

SNPshotrs587779234
SNPdbers587779234
MSV3drs587779234
GWAS Ctlgrs587779234
Max Magnitude0
ClinVar
Risk rs587779234(A;A)
Alt rs587779234(A;A)
Reference rs587779234(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027452G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074736.2,