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rs863225389

From SNPedia

Orientationplus
Make rs863225389(-;-)
Make rs863225389(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47445573
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225389
ebirs863225389
HLIrs863225389
Exacrs863225389
Varsomers863225389
Maprs863225389
PheGenIrs863225389
hapmaprs863225389
1000 genomesrs863225389
hgdprs863225389
ensemblrs863225389
gopubmedrs863225389
geneviewrs863225389
scholarrs863225389
googlers863225389
pharmgkbrs863225389
gwascentralrs863225389
openSNPrs863225389
23andMers863225389
23andMe allrs863225389
SNP Nexus

SNPshotrs863225389
SNPdbers863225389
MSV3drs863225389
GWAS Ctlgrs863225389
Max Magnitude
ClinVar
Risk rs863225389(;)
Alt rs863225389(;)
Reference rs863225389(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47672712delA
CLNSRC
CLNACC RCV000202110.1,