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rs876661025

From SNPedia

Orientationplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs876661025(-;-)
Make rs876661025(-;AC)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800252
GeneMSH6
is asnp
is mentioned by
dbSNPrs876661025
ebirs876661025
HLIrs876661025
Exacrs876661025
Varsomers876661025
Maprs876661025
PheGenIrs876661025
hapmaprs876661025
1000 genomesrs876661025
hgdprs876661025
ensemblrs876661025
gopubmedrs876661025
geneviewrs876661025
scholarrs876661025
googlers876661025
pharmgkbrs876661025
gwascentralrs876661025
openSNPrs876661025
23andMers876661025
23andMe allrs876661025
SNP Nexus

SNPshotrs876661025
SNPdbers876661025
MSV3drs876661025
GWAS Ctlgrs876661025
Max Magnitude0
ClinVar
Risk rs876661025(;)
Alt rs876661025(;)
Reference rs876661025(AC;AC)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48027391_48027392delAC
CLNSRC
CLNACC RCV000216101.1,