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rs863225409

From SNPedia

Orientationplus
Make rs863225409(-;-)
Make rs863225409(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47805687
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225409
ebirs863225409
HLIrs863225409
Exacrs863225409
Varsomers863225409
Maprs863225409
PheGenIrs863225409
hapmaprs863225409
1000 genomesrs863225409
hgdprs863225409
ensemblrs863225409
gopubmedrs863225409
geneviewrs863225409
scholarrs863225409
googlers863225409
pharmgkbrs863225409
gwascentralrs863225409
openSNPrs863225409
23andMers863225409
23andMe allrs863225409
SNP Nexus

SNPshotrs863225409
SNPdbers863225409
MSV3drs863225409
GWAS Ctlgrs863225409
Max Magnitude
ClinVar
Risk rs863225409(;)
Alt rs863225409(;)
Reference rs863225409(TG;TG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48032826_48032827delTG
CLNSRC
CLNACC RCV000202124.1,