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rs587779247

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779247(-;-)
Make rs587779247(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800748
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779247
ebirs587779247
HLIrs587779247
Exacrs587779247
Varsomers587779247
Maprs587779247
PheGenIrs587779247
hapmaprs587779247
1000 genomesrs587779247
hgdprs587779247
ensemblrs587779247
gopubmedrs587779247
geneviewrs587779247
scholarrs587779247
googlers587779247
pharmgkbrs587779247
gwascentralrs587779247
openSNPrs587779247
23andMers587779247
23andMe allrs587779247
SNP Nexus

SNPshotrs587779247
SNPdbers587779247
MSV3drs587779247
GWAS Ctlgrs587779247
Max Magnitude0
ClinVar
Risk rs587779247(;)
Alt rs587779247(;)
Reference rs587779247(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027887delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074780.2,