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rs876661073

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876661073(-;-)
Make rs876661073(-;T)
Make rs876661073(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47804962
GeneMSH6
is asnp
is mentioned by
dbSNPrs876661073
ebirs876661073
HLIrs876661073
Exacrs876661073
Varsomers876661073
Maprs876661073
PheGenIrs876661073
hapmaprs876661073
1000 genomesrs876661073
hgdprs876661073
ensemblrs876661073
gopubmedrs876661073
geneviewrs876661073
scholarrs876661073
googlers876661073
pharmgkbrs876661073
gwascentralrs876661073
openSNPrs876661073
23andMers876661073
23andMe allrs876661073
SNP Nexus

SNPshotrs876661073
SNPdbers876661073
MSV3drs876661073
GWAS Ctlgrs876661073
Max Magnitude0
ClinVar
Risk rs876661073(T;T)
Alt rs876661073(T;T)
Reference rs876661073(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48032101dupT
CLNSRC
CLNACC RCV000222529.1,