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rs876658996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658996(G;G)
Make rs876658996(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47410374
GeneMSH2
is asnp
is mentioned by
dbSNPrs876658996
dbSNP (old)rs876658996
ClinGenrs876658996
ebirs876658996
HLIrs876658996
Exacrs876658996
Gnomadrs876658996
Varsomers876658996
Maprs876658996
PheGenIrs876658996
Biobankrs876658996
1000 genomesrs876658996
hgdprs876658996
ensemblrs876658996
gopubmedrs876658996
geneviewrs876658996
scholarrs876658996
googlers876658996
pharmgkbrs876658996
gwascentralrs876658996
openSNPrs876658996
23andMers876658996
23andMe allrs876658996
SNP Nexus

SNPshotrs876658996
SNPdbers876658996
MSV3drs876658996
GWAS Ctlgrs876658996
Max Magnitude0
ClinVar
Risk rs876658996(G;G)
Alt rs876658996(G;G)
Reference Rs876658996(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47637513T>G
CLNSRC
CLNACC RCV000218166.2,