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rs876661125

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661125(-;-)
Make rs876661125(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47791124
GeneMSH6
is asnp
is mentioned by
dbSNPrs876661125
ebirs876661125
HLIrs876661125
Exacrs876661125
Varsomers876661125
Maprs876661125
PheGenIrs876661125
hapmaprs876661125
1000 genomesrs876661125
hgdprs876661125
ensemblrs876661125
gopubmedrs876661125
geneviewrs876661125
scholarrs876661125
googlers876661125
pharmgkbrs876661125
gwascentralrs876661125
openSNPrs876661125
23andMers876661125
23andMe allrs876661125
SNP Nexus

SNPshotrs876661125
SNPdbers876661125
MSV3drs876661125
GWAS Ctlgrs876661125
Max Magnitude0
ClinVar
Risk rs876661125(;)
Alt rs876661125(;)
Reference rs876661125(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48018263delG
CLNSRC
CLNACC RCV000216047.1,