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rs730881827

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs730881827(-;-)
Make rs730881827(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800815
GeneMSH6
is asnp
is mentioned by
dbSNPrs730881827
ebirs730881827
HLIrs730881827
Exacrs730881827
Varsomers730881827
Maprs730881827
PheGenIrs730881827
hapmaprs730881827
1000 genomesrs730881827
hgdprs730881827
ensemblrs730881827
gopubmedrs730881827
geneviewrs730881827
scholarrs730881827
googlers730881827
pharmgkbrs730881827
gwascentralrs730881827
openSNPrs730881827
23andMers730881827
23andMe allrs730881827
SNP Nexus

SNPshotrs730881827
SNPdbers730881827
MSV3drs730881827
GWAS Ctlgrs730881827
Max Magnitude0
ClinVar
Risk rs730881827(;)
Alt rs730881827(;)
Reference rs730881827(AA;AA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48027954_48027955delAA
CLNSRC
CLNACC RCV000160743.2,