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rs587779267

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779267(G;T)
Make rs587779267(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47804958
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779267
ebirs587779267
HLIrs587779267
Exacrs587779267
Varsomers587779267
Maprs587779267
PheGenIrs587779267
hapmaprs587779267
1000 genomesrs587779267
hgdprs587779267
ensemblrs587779267
gopubmedrs587779267
geneviewrs587779267
scholarrs587779267
googlers587779267
pharmgkbrs587779267
gwascentralrs587779267
openSNPrs587779267
23andMers587779267
23andMe allrs587779267
SNP Nexus

SNPshotrs587779267
SNPdbers587779267
MSV3drs587779267
GWAS Ctlgrs587779267
Max Magnitude0
ClinVar
Risk rs587779267(T;T)
Alt rs587779267(T;T)
Reference rs587779267(G;G)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48032097G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074867.2, RCV000115417.2,