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rs863225394

From SNPedia

Orientationplus
Make rs863225394(-;-)
Make rs863225394(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47478358
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225394
ebirs863225394
HLIrs863225394
Exacrs863225394
Varsomers863225394
Maprs863225394
PheGenIrs863225394
hapmaprs863225394
1000 genomesrs863225394
hgdprs863225394
ensemblrs863225394
gopubmedrs863225394
geneviewrs863225394
scholarrs863225394
googlers863225394
pharmgkbrs863225394
gwascentralrs863225394
openSNPrs863225394
23andMers863225394
23andMe allrs863225394
SNP Nexus

SNPshotrs863225394
SNPdbers863225394
MSV3drs863225394
GWAS Ctlgrs863225394
Max Magnitude
ClinVar
Risk rs863225394(;)
Alt rs863225394(;)
Reference rs863225394(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47705497delT
CLNSRC
CLNACC RCV000201981.1,