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rs863225411

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225411(-;AGAA)
Make rs863225411(AGAA;AGAA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47806259
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225411
ClinGenrs863225411
ebirs863225411
HLIrs863225411
Exacrs863225411
Varsomers863225411
Maprs863225411
PheGenIrs863225411
hapmaprs863225411
1000 genomesrs863225411
hgdprs863225411
ensemblrs863225411
gopubmedrs863225411
geneviewrs863225411
scholarrs863225411
googlers863225411
pharmgkbrs863225411
gwascentralrs863225411
openSNPrs863225411
23andMers863225411
23andMe allrs863225411
SNP Nexus

SNPshotrs863225411
SNPdbers863225411
MSV3drs863225411
GWAS Ctlgrs863225411
Max Magnitude0
ClinVar
Risk rs863225411(AAAG;AAAG)
Alt rs863225411(AAAG;AAAG)
Reference Rs863225411(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48033395_48033398dupAGAA
CLNSRC
CLNACC RCV000202173.1,