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rs587779315

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779315(A;T)
Make rs587779315(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47798635
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779315
ebirs587779315
HLIrs587779315
Exacrs587779315
Varsomers587779315
Maprs587779315
PheGenIrs587779315
hapmaprs587779315
1000 genomesrs587779315
hgdprs587779315
ensemblrs587779315
gopubmedrs587779315
geneviewrs587779315
scholarrs587779315
googlers587779315
pharmgkbrs587779315
gwascentralrs587779315
openSNPrs587779315
23andMers587779315
23andMe allrs587779315
SNP Nexus

SNPshotrs587779315
SNPdbers587779315
MSV3drs587779315
GWAS Ctlgrs587779315
Max Magnitude0
ClinVar
Risk rs587779315(T;T)
Alt rs587779315(T;T)
Reference rs587779315(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025774A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075019.2,