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rs863225408

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GACTT;GACTT) 0 common in clinvar
Make rs863225408(-;-)
Make rs863225408(-;ACTTG)
Make rs863225408(ACTTG;ACTTG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47804999
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225408
ClinGenrs863225408
ebirs863225408
HLIrs863225408
Exacrs863225408
Varsomers863225408
Maprs863225408
PheGenIrs863225408
hapmaprs863225408
1000 genomesrs863225408
hgdprs863225408
ensemblrs863225408
gopubmedrs863225408
geneviewrs863225408
scholarrs863225408
googlers863225408
pharmgkbrs863225408
gwascentralrs863225408
openSNPrs863225408
23andMers863225408
23andMe allrs863225408
SNP Nexus

SNPshotrs863225408
SNPdbers863225408
MSV3drs863225408
GWAS Ctlgrs863225408
Max Magnitude0
ClinVar
Risk rs863225408(-;-)
Alt rs863225408(-;-)
Reference Rs863225408(GACTT;GACTT)
Significance Other
Disease not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48032138_48032142delACTTG
CLNSRC
CLNACC RCV000202131.1, RCV000233857.2, RCV000491652.1,