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rs587779263

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779263(G;T)
Make rs587779263(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47804909
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779263
ebirs587779263
HLIrs587779263
Exacrs587779263
Varsomers587779263
Maprs587779263
PheGenIrs587779263
hapmaprs587779263
1000 genomesrs587779263
hgdprs587779263
ensemblrs587779263
gopubmedrs587779263
geneviewrs587779263
scholarrs587779263
googlers587779263
pharmgkbrs587779263
gwascentralrs587779263
openSNPrs587779263
23andMers587779263
23andMe allrs587779263
SNP Nexus

SNPshotrs587779263
SNPdbers587779263
MSV3drs587779263
GWAS Ctlgrs587779263
Max Magnitude0
ClinVar
Risk rs587779263(T;T)
Alt rs587779263(T;T)
Reference rs587779263(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.48032048G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074858.2, RCV000215652.1,