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

rs587783053

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783053(-;-)
Make rs587783053(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47478365
GeneMSH2
is asnp
is mentioned by
dbSNPrs587783053
ebirs587783053
HLIrs587783053
Exacrs587783053
Varsomers587783053
Maprs587783053
PheGenIrs587783053
hapmaprs587783053
1000 genomesrs587783053
hgdprs587783053
ensemblrs587783053
gopubmedrs587783053
geneviewrs587783053
scholarrs587783053
googlers587783053
pharmgkbrs587783053
gwascentralrs587783053
openSNPrs587783053
23andMers587783053
23andMe allrs587783053
SNP Nexus

SNPshotrs587783053
SNPdbers587783053
MSV3drs587783053
GWAS Ctlgrs587783053
Max Magnitude0
ClinVar
Risk rs587783053(;)
Alt rs587783053(;)
Reference rs587783053(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome I
Variation info
Gene MSH2
CLNDBN Lynch syndrome I
Reversed 0
HGVS NC_000002.11:g.47705504delA
CLNSRC
CLNACC RCV000144618.1,