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rs863225391

From SNPedia

Orientationplus
Make rs863225391(-;-)
Make rs863225391(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47466685
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225391
ebirs863225391
HLIrs863225391
Exacrs863225391
Varsomers863225391
Maprs863225391
PheGenIrs863225391
hapmaprs863225391
1000 genomesrs863225391
hgdprs863225391
ensemblrs863225391
gopubmedrs863225391
geneviewrs863225391
scholarrs863225391
googlers863225391
pharmgkbrs863225391
gwascentralrs863225391
openSNPrs863225391
23andMers863225391
23andMe allrs863225391
SNP Nexus

SNPshotrs863225391
SNPdbers863225391
MSV3drs863225391
GWAS Ctlgrs863225391
Max Magnitude
ClinVar
Risk rs863225391(;)
Alt rs863225391(;)
Reference rs863225391(TG;TG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47693824_47693825delTG
CLNSRC
CLNACC RCV000202016.1,