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rs876661033

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661033(-;-)
Make rs876661033(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47799628
GeneMSH6
is asnp
is mentioned by
dbSNPrs876661033
ebirs876661033
HLIrs876661033
Exacrs876661033
Varsomers876661033
Maprs876661033
PheGenIrs876661033
hapmaprs876661033
1000 genomesrs876661033
hgdprs876661033
ensemblrs876661033
gopubmedrs876661033
geneviewrs876661033
scholarrs876661033
googlers876661033
pharmgkbrs876661033
gwascentralrs876661033
openSNPrs876661033
23andMers876661033
23andMe allrs876661033
SNP Nexus

SNPshotrs876661033
SNPdbers876661033
MSV3drs876661033
GWAS Ctlgrs876661033
Max Magnitude0
ClinVar
Risk rs876661033(;)
Alt rs876661033(;)
Reference rs876661033(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48026767delT
CLNSRC
CLNACC RCV000214419.1,