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rs1064797108

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome1
Position22661024
GeneC1QB
is asnp
is mentioned by
dbSNPrs1064797108
dbSNP (old)rs1064797108
ClinGenrs1064797108
ebirs1064797108
HLIrs1064797108
Exacrs1064797108
Gnomadrs1064797108
Varsomers1064797108
LitVarrs1064797108
Maprs1064797108
PheGenIrs1064797108
Biobankrs1064797108
1000 genomesrs1064797108
hgdprs1064797108
ensemblrs1064797108
gopubmedrs1064797108
geneviewrs1064797108
scholarrs1064797108
googlers1064797108
pharmgkbrs1064797108
gwascentralrs1064797108
openSNPrs1064797108
23andMers1064797108
23andMe allrs1064797108
SNPshotrs1064797108
SNPdbers1064797108
MSV3drs1064797108
GWAS Ctlgrs1064797108
Max Magnitude0
ClinVar
Risk rs1064797108(-;-)
Alt rs1064797108(-;-)
Reference Rs1064797108(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C1QB
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.22987517delC
CLNSRC
CLNACC RCV000488091.1,