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

rs587783055

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587783055(-;-)
Make rs587783055(-;A)
Make rs587783055(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47429936
GeneMSH2
is asnp
is mentioned by
dbSNPrs587783055
ebirs587783055
HLIrs587783055
Exacrs587783055
Varsomers587783055
Maprs587783055
PheGenIrs587783055
hapmaprs587783055
1000 genomesrs587783055
hgdprs587783055
ensemblrs587783055
gopubmedrs587783055
geneviewrs587783055
scholarrs587783055
googlers587783055
pharmgkbrs587783055
gwascentralrs587783055
openSNPrs587783055
23andMers587783055
23andMe allrs587783055
SNP Nexus

SNPshotrs587783055
SNPdbers587783055
MSV3drs587783055
GWAS Ctlgrs587783055
Max Magnitude0
ClinVar
Risk rs587783055(A;A)
Alt rs587783055(A;A)
Reference rs587783055(;)
Significance Pathogenic
Disease Lynch syndrome I
Variation info
Gene MSH2
CLNDBN Lynch syndrome I
Reversed 0
HGVS NC_000002.11:g.47657075dupA
CLNSRC
CLNACC RCV000144623.1,