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rs1064794384

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Chromosome2
Position47806273
GeneMSH6
is asnp
is mentioned by
dbSNPrs1064794384
dbSNP (old)rs1064794384
ClinGenrs1064794384
ebirs1064794384
HLIrs1064794384
Exacrs1064794384
Gnomadrs1064794384
Varsomers1064794384
Maprs1064794384
PheGenIrs1064794384
Biobankrs1064794384
1000 genomesrs1064794384
hgdprs1064794384
ensemblrs1064794384
gopubmedrs1064794384
geneviewrs1064794384
scholarrs1064794384
googlers1064794384
pharmgkbrs1064794384
gwascentralrs1064794384
openSNPrs1064794384
23andMers1064794384
23andMe allrs1064794384
SNPshotrs1064794384
SNPdbers1064794384
MSV3drs1064794384
GWAS Ctlgrs1064794384
Max Magnitude0
ClinVar
Risk rs1064794384(-;-)
Alt rs1064794384(-;-)
Reference Rs1064794384(TA;TA)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48033412_48033413delTA
CLNSRC
CLNACC RCV000482291.1,