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rs863225400

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs863225400(-;-)
Make rs863225400(-;GA)
Make rs863225400(GA;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799473
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225400
dbSNP (old)rs863225400
ClinGenrs863225400
ebirs863225400
HLIrs863225400
Exacrs863225400
Gnomadrs863225400
Varsomers863225400
Maprs863225400
PheGenIrs863225400
Biobankrs863225400
1000 genomesrs863225400
hgdprs863225400
ensemblrs863225400
gopubmedrs863225400
geneviewrs863225400
scholarrs863225400
googlers863225400
pharmgkbrs863225400
gwascentralrs863225400
openSNPrs863225400
23andMers863225400
23andMe allrs863225400
SNP Nexus

SNPshotrs863225400
SNPdbers863225400
MSV3drs863225400
GWAS Ctlgrs863225400
Max Magnitude0
ClinVar
Risk rs863225400(-;-)
Alt rs863225400(-;-)
Reference Rs863225400(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48026612_48026613delGA
CLNSRC
CLNACC RCV000202087.1,