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rs587779256

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587779256(-;-)
Make rs587779256(-;GA)
Make rs587779256(GA;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47803419
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779256
ebirs587779256
HLIrs587779256
Exacrs587779256
Varsomers587779256
Maprs587779256
PheGenIrs587779256
hapmaprs587779256
1000 genomesrs587779256
hgdprs587779256
ensemblrs587779256
gopubmedrs587779256
geneviewrs587779256
scholarrs587779256
googlers587779256
pharmgkbrs587779256
gwascentralrs587779256
openSNPrs587779256
23andMers587779256
23andMe allrs587779256
SNP Nexus

SNPshotrs587779256
SNPdbers587779256
MSV3drs587779256
GWAS Ctlgrs587779256
Max Magnitude0
ClinVar
Risk rs587779256(;)
Alt rs587779256(;)
Reference rs587779256(AG;AG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030558_48030559delGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074812.2,