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rs730881824

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs730881824(-;-)
Make rs730881824(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47796036
GeneMSH6
is asnp
is mentioned by
dbSNPrs730881824
ebirs730881824
HLIrs730881824
Exacrs730881824
Varsomers730881824
Maprs730881824
PheGenIrs730881824
hapmaprs730881824
1000 genomesrs730881824
hgdprs730881824
ensemblrs730881824
gopubmedrs730881824
geneviewrs730881824
scholarrs730881824
googlers730881824
pharmgkbrs730881824
gwascentralrs730881824
openSNPrs730881824
23andMers730881824
23andMe allrs730881824
SNP Nexus

SNPshotrs730881824
SNPdbers730881824
MSV3drs730881824
GWAS Ctlgrs730881824
Max Magnitude0
ClinVar
Risk rs730881824(;)
Alt rs730881824(;)
Reference rs730881824(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48023177_48023178delAG
CLNSRC
CLNACC RCV000115436.3,