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rs878853802

From SNPedia

Orientationplus
Geno Mag Summary
(CCTTGTA;CCTTGTA) 0 common in clinvar
Make rs878853802(-;-)
Make rs878853802(-;CCTTGTA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47463048
GeneMSH2
is asnp
is mentioned by
dbSNPrs878853802
ebirs878853802
HLIrs878853802
Exacrs878853802
Varsomers878853802
Maprs878853802
PheGenIrs878853802
hapmaprs878853802
1000 genomesrs878853802
hgdprs878853802
ensemblrs878853802
gopubmedrs878853802
geneviewrs878853802
scholarrs878853802
googlers878853802
pharmgkbrs878853802
gwascentralrs878853802
openSNPrs878853802
23andMers878853802
23andMe allrs878853802
SNP Nexus

SNPshotrs878853802
SNPdbers878853802
MSV3drs878853802
GWAS Ctlgrs878853802
Max Magnitude0
ClinVar
Risk rs878853802(;)
Alt rs878853802(;)
Reference rs878853802(CCTTGTA;CCTTGTA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690187_47690193delCCTTGTA
CLNSRC
CLNACC RCV000232666.1,