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rs587779945

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587779945(-;-)
Make rs587779945(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47796038
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779945
ebirs587779945
HLIrs587779945
Exacrs587779945
Varsomers587779945
Maprs587779945
PheGenIrs587779945
hapmaprs587779945
1000 genomesrs587779945
hgdprs587779945
ensemblrs587779945
gopubmedrs587779945
geneviewrs587779945
scholarrs587779945
googlers587779945
pharmgkbrs587779945
gwascentralrs587779945
openSNPrs587779945
23andMers587779945
23andMe allrs587779945
SNP Nexus

SNPshotrs587779945
SNPdbers587779945
MSV3drs587779945
GWAS Ctlgrs587779945
Max Magnitude0
ClinVar
Risk rs587779945(;)
Alt rs587779945(;)
Reference rs587779945(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,