Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779119

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs587779119(-;-)
Make rs587779119(-;TA)
Make rs587779119(TA;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47475245
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779119
ebirs587779119
HLIrs587779119
Exacrs587779119
Varsomers587779119
Maprs587779119
PheGenIrs587779119
hapmaprs587779119
1000 genomesrs587779119
hgdprs587779119
ensemblrs587779119
gopubmedrs587779119
geneviewrs587779119
scholarrs587779119
googlers587779119
pharmgkbrs587779119
gwascentralrs587779119
openSNPrs587779119
23andMers587779119
23andMe allrs587779119
SNP Nexus

SNPshotrs587779119
SNPdbers587779119
MSV3drs587779119
GWAS Ctlgrs587779119
Max Magnitude0
ClinVar
Risk rs587779119(;)
Alt rs587779119(;)
Reference rs587779119(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702384_47702385delTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076328.2,