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rs1064793185

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAAACGCCCTC;GAAACGCCCTC) 0 common in clinvar
Chromosome2
Position47798935
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064793185
dbSNP (old)rs1064793185
ClinGenrs1064793185
ebirs1064793185
HLIrs1064793185
Exacrs1064793185
Gnomadrs1064793185
Varsomers1064793185
Maprs1064793185
PheGenIrs1064793185
Biobankrs1064793185
1000 genomesrs1064793185
hgdprs1064793185
ensemblrs1064793185
gopubmedrs1064793185
geneviewrs1064793185
scholarrs1064793185
googlers1064793185
pharmgkbrs1064793185
gwascentralrs1064793185
openSNPrs1064793185
23andMers1064793185
23andMe allrs1064793185
SNPshotrs1064793185
SNPdbers1064793185
MSV3drs1064793185
GWAS Ctlgrs1064793185
Max Magnitude0
ClinVar
Risk rs1064793185(-;-)
Alt rs1064793185(-;-)
Reference Rs1064793185(GAAACGCCCTC;GAAACGCCCTC)
Significance Pathogenic
Disease not provided Hereditary nonpolyposis colorectal carcinoma
Variation info
Gene MSH6
CLNDBN not provided Hereditary nonpolyposis colorectal carcinoma
Reversed 0
HGVS NC_000002.11:g.48026074_48026084delGAAACGCCCTC
CLNSRC
CLNACC RCV000478431.1, RCV000490670.1,