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rs1064793380

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome8
Position116848999
GeneRAD21
is asnp
is mentioned by
dbSNPrs1064793380
dbSNP (old)rs1064793380
ClinGenrs1064793380
ebirs1064793380
HLIrs1064793380
Exacrs1064793380
Gnomadrs1064793380
Varsomers1064793380
LitVarrs1064793380
Maprs1064793380
PheGenIrs1064793380
Biobankrs1064793380
1000 genomesrs1064793380
hgdprs1064793380
ensemblrs1064793380
gopubmedrs1064793380
geneviewrs1064793380
scholarrs1064793380
googlers1064793380
pharmgkbrs1064793380
gwascentralrs1064793380
openSNPrs1064793380
23andMers1064793380
23andMe allrs1064793380
SNPshotrs1064793380
SNPdbers1064793380
MSV3drs1064793380
GWAS Ctlgrs1064793380
Max Magnitude0
ClinVar
Risk rs1064793380(-;-)
Alt rs1064793380(-;-)
Reference Rs1064793380(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RAD21
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.117861238delG
CLNSRC
CLNACC RCV000479864.1,