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rs730881828

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881828(-;-)
Make rs730881828(-;AC)
Make rs730881828(AC;AC)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47804995
GeneMSH6
is asnp
is mentioned by
dbSNPrs730881828
ebirs730881828
HLIrs730881828
Exacrs730881828
Varsomers730881828
Maprs730881828
PheGenIrs730881828
hapmaprs730881828
1000 genomesrs730881828
hgdprs730881828
ensemblrs730881828
gopubmedrs730881828
geneviewrs730881828
scholarrs730881828
googlers730881828
pharmgkbrs730881828
gwascentralrs730881828
openSNPrs730881828
23andMers730881828
23andMe allrs730881828
SNP Nexus

SNPshotrs730881828
SNPdbers730881828
MSV3drs730881828
GWAS Ctlgrs730881828
Max Magnitude0
ClinVar
Risk rs730881828(AC;AC)
Alt rs730881828(AC;AC)
Reference rs730881828(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48032133_48032134dupAC
CLNSRC
CLNACC RCV000160744.1,