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rs1064793183

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position47783488
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064793183
dbSNP (old)rs1064793183
ClinGenrs1064793183
ebirs1064793183
HLIrs1064793183
Exacrs1064793183
Gnomadrs1064793183
Varsomers1064793183
LitVarrs1064793183
Maprs1064793183
PheGenIrs1064793183
Biobankrs1064793183
1000 genomesrs1064793183
hgdprs1064793183
ensemblrs1064793183
gopubmedrs1064793183
geneviewrs1064793183
scholarrs1064793183
googlers1064793183
pharmgkbrs1064793183
gwascentralrs1064793183
openSNPrs1064793183
23andMers1064793183
23andMe allrs1064793183
SNPshotrs1064793183
SNPdbers1064793183
MSV3drs1064793183
GWAS Ctlgrs1064793183
Max Magnitude0
ClinVar
Risk rs1064793183(-;-)
Alt rs1064793183(-;-)
Reference Rs1064793183(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48010627delC
CLNSRC
CLNACC RCV000479132.1,