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rs1064794798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome4
Position15601288
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs1064794798
dbSNP (old)rs1064794798
ClinGenrs1064794798
ebirs1064794798
HLIrs1064794798
Exacrs1064794798
Gnomadrs1064794798
Varsomers1064794798
LitVarrs1064794798
Maprs1064794798
PheGenIrs1064794798
Biobankrs1064794798
1000 genomesrs1064794798
hgdprs1064794798
ensemblrs1064794798
gopubmedrs1064794798
geneviewrs1064794798
scholarrs1064794798
googlers1064794798
pharmgkbrs1064794798
gwascentralrs1064794798
openSNPrs1064794798
23andMers1064794798
23andMe allrs1064794798
SNPshotrs1064794798
SNPdbers1064794798
MSV3drs1064794798
GWAS Ctlgrs1064794798
Max Magnitude0
ClinVar
Risk rs1064794798(C;C)
Alt rs1064794798(C;C)
Reference Rs1064794798(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CC2D2A
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.15602911G>C
CLNSRC
CLNACC RCV000482125.1,