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rs863225385

From SNPedia

Orientationplus
Make rs863225385(-;-)
Make rs863225385(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47429755
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225385
ebirs863225385
HLIrs863225385
Exacrs863225385
Varsomers863225385
Maprs863225385
PheGenIrs863225385
hapmaprs863225385
1000 genomesrs863225385
hgdprs863225385
ensemblrs863225385
gopubmedrs863225385
geneviewrs863225385
scholarrs863225385
googlers863225385
pharmgkbrs863225385
gwascentralrs863225385
openSNPrs863225385
23andMers863225385
23andMe allrs863225385
SNP Nexus

SNPshotrs863225385
SNPdbers863225385
MSV3drs863225385
GWAS Ctlgrs863225385
Max Magnitude
ClinVar
Risk rs863225385(;)
Alt rs863225385(;)
Reference rs863225385(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47656894delG
CLNSRC
CLNACC RCV000202167.1,