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rs1064793598

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome10
Position110590441
GeneSMC3
is asnp
is mentioned by
dbSNPrs1064793598
dbSNP (old)rs1064793598
ClinGenrs1064793598
ebirs1064793598
HLIrs1064793598
Exacrs1064793598
Gnomadrs1064793598
Varsomers1064793598
Maprs1064793598
PheGenIrs1064793598
Biobankrs1064793598
1000 genomesrs1064793598
hgdprs1064793598
ensemblrs1064793598
gopubmedrs1064793598
geneviewrs1064793598
scholarrs1064793598
googlers1064793598
pharmgkbrs1064793598
gwascentralrs1064793598
openSNPrs1064793598
23andMers1064793598
23andMe allrs1064793598
SNPshotrs1064793598
SNPdbers1064793598
MSV3drs1064793598
GWAS Ctlgrs1064793598
Max Magnitude0
ClinVar
Risk rs1064793598(-;-)
Alt rs1064793598(-;-)
Reference Rs1064793598(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SMC3
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.112350199delC
CLNSRC
CLNACC RCV000484165.1,