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rs863225401

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225401(A;A)
Make rs863225401(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799866
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225401
ebirs863225401
HLIrs863225401
Exacrs863225401
Varsomers863225401
Maprs863225401
PheGenIrs863225401
hapmaprs863225401
1000 genomesrs863225401
hgdprs863225401
ensemblrs863225401
gopubmedrs863225401
geneviewrs863225401
scholarrs863225401
googlers863225401
pharmgkbrs863225401
gwascentralrs863225401
openSNPrs863225401
23andMers863225401
23andMe allrs863225401
SNP Nexus

SNPshotrs863225401
SNPdbers863225401
MSV3drs863225401
GWAS Ctlgrs863225401
Max Magnitude0
ClinVar
Risk rs863225401(A;A)
Alt rs863225401(A;A)
Reference rs863225401(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48027005G>A
CLNSRC
CLNACC RCV000202222.1,