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rs587779979

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779979(-;-)
Make rs587779979(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47414408
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779979
ebirs587779979
HLIrs587779979
Exacrs587779979
Varsomers587779979
Maprs587779979
PheGenIrs587779979
hapmaprs587779979
1000 genomesrs587779979
hgdprs587779979
ensemblrs587779979
gopubmedrs587779979
geneviewrs587779979
scholarrs587779979
googlers587779979
pharmgkbrs587779979
gwascentralrs587779979
openSNPrs587779979
23andMers587779979
23andMe allrs587779979
SNP Nexus

SNPshotrs587779979
SNPdbers587779979
MSV3drs587779979
GWAS Ctlgrs587779979
Max Magnitude0
ClinVar
Risk rs587779979(;)
Alt rs587779979(;)
Reference rs587779979(A;A)
Significance Pathogenic
Disease not provided Lynch syndrome
Variation info
Gene MSH2
CLNDBN not provided Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641547delA
CLNSRC
CLNACC RCV000115548.3, RCV000232943.1,