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rs587779203

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779203(-;-)
Make rs587779203(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799084
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779203
ebirs587779203
HLIrs587779203
Exacrs587779203
Varsomers587779203
Maprs587779203
PheGenIrs587779203
hapmaprs587779203
1000 genomesrs587779203
hgdprs587779203
ensemblrs587779203
gopubmedrs587779203
geneviewrs587779203
scholarrs587779203
googlers587779203
pharmgkbrs587779203
gwascentralrs587779203
openSNPrs587779203
23andMers587779203
23andMe allrs587779203
SNP Nexus

SNPshotrs587779203
SNPdbers587779203
MSV3drs587779203
GWAS Ctlgrs587779203
Max Magnitude0
ClinVar
Risk rs587779203(;)
Alt rs587779203(;)
Reference rs587779203(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026223delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074632.2,