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rs1064793489

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position47805028
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064793489
dbSNP (old)rs1064793489
ClinGenrs1064793489
ebirs1064793489
HLIrs1064793489
Exacrs1064793489
Gnomadrs1064793489
Varsomers1064793489
Maprs1064793489
PheGenIrs1064793489
Biobankrs1064793489
1000 genomesrs1064793489
hgdprs1064793489
ensemblrs1064793489
gopubmedrs1064793489
geneviewrs1064793489
scholarrs1064793489
googlers1064793489
pharmgkbrs1064793489
gwascentralrs1064793489
openSNPrs1064793489
23andMers1064793489
23andMe allrs1064793489
SNPshotrs1064793489
SNPdbers1064793489
MSV3drs1064793489
GWAS Ctlgrs1064793489
Max Magnitude0
ClinVar
Risk rs1064793489(-;-)
Alt rs1064793489(-;-)
Reference Rs1064793489(G;G)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48032167delG
CLNSRC
CLNACC RCV000480410.1, RCV000491243.1,