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rs587779255

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779255(G;T)
Make rs587779255(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47801156
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779255
ebirs587779255
HLIrs587779255
Exacrs587779255
Varsomers587779255
Maprs587779255
PheGenIrs587779255
hapmaprs587779255
1000 genomesrs587779255
hgdprs587779255
ensemblrs587779255
gopubmedrs587779255
geneviewrs587779255
scholarrs587779255
googlers587779255
pharmgkbrs587779255
gwascentralrs587779255
openSNPrs587779255
23andMers587779255
23andMe allrs587779255
SNP Nexus

SNPshotrs587779255
SNPdbers587779255
MSV3drs587779255
GWAS Ctlgrs587779255
Max Magnitude0
ClinVar
Risk rs587779255(T;T)
Alt rs587779255(T;T)
Reference rs587779255(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48028295G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074809.3,