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rs587779319

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779319(-;-)
Make rs587779319(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47798693
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779319
ebirs587779319
HLIrs587779319
Exacrs587779319
Varsomers587779319
Maprs587779319
PheGenIrs587779319
hapmaprs587779319
1000 genomesrs587779319
hgdprs587779319
ensemblrs587779319
gopubmedrs587779319
geneviewrs587779319
scholarrs587779319
googlers587779319
pharmgkbrs587779319
gwascentralrs587779319
openSNPrs587779319
23andMers587779319
23andMe allrs587779319
SNP Nexus

SNPshotrs587779319
SNPdbers587779319
MSV3drs587779319
GWAS Ctlgrs587779319
Max Magnitude0
ClinVar
Risk rs587779319(;)
Alt rs587779319(;)
Reference rs587779319(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025832delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075027.2,