Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs863225403(-;-)
Make rs863225403(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47800788
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225403
dbSNP (old)rs863225403
ClinGenrs863225403
ebirs863225403
HLIrs863225403
Exacrs863225403
Gnomadrs863225403
Varsomers863225403
Maprs863225403
PheGenIrs863225403
Biobankrs863225403
1000 genomesrs863225403
hgdprs863225403
ensemblrs863225403
gopubmedrs863225403
geneviewrs863225403
scholarrs863225403
googlers863225403
pharmgkbrs863225403
gwascentralrs863225403
openSNPrs863225403
23andMers863225403
23andMe allrs863225403
SNP Nexus

SNPshotrs863225403
SNPdbers863225403
MSV3drs863225403
GWAS Ctlgrs863225403
Max Magnitude0
ClinVar
Risk rs863225403(-;-)
Alt rs863225403(-;-)
Reference Rs863225403(TG;TG)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48027927_48027928delTG
CLNSRC
CLNACC RCV000202273.1, RCV000491348.1,