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rs539992721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs539992721(G;G)
Make rs539992721(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position6719285
GeneC3
is asnp
is mentioned by
dbSNPrs539992721
dbSNP (classic)rs539992721
ClinGenrs539992721
ebirs539992721
HLIrs539992721
Exacrs539992721
Gnomadrs539992721
Varsomers539992721
LitVarrs539992721
Maprs539992721
PheGenIrs539992721
Biobankrs539992721
1000 genomesrs539992721
hgdprs539992721
ensemblrs539992721
geneviewrs539992721
scholarrs539992721
googlers539992721
pharmgkbrs539992721
gwascentralrs539992721
openSNPrs539992721
23andMers539992721
23andMe allrs539992721
SNPshotrs539992721
SNPdbers539992721
MSV3drs539992721
GWAS Ctlgrs539992721
Max Magnitude0
ClinVar
Risk rs539992721(G;G)
Alt rs539992721(G;G)
Reference Rs539992721(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C3
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.6719296T>G
CLNSRC
CLNACC RCV000427027.1,