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rs10947223

From SNPedia

Orientationplus
Stabilizedplus
Make rs10947223(A;A)
Make rs10947223(A;G)
Make rs10947223(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position31904606
GeneC2
is asnp
is mentioned by
dbSNPrs10947223
dbSNP (old)rs10947223
ClinGenrs10947223
ebirs10947223
HLIrs10947223
Exacrs10947223
Gnomadrs10947223
Varsomers10947223
LitVarrs10947223
Maprs10947223
PheGenIrs10947223
Biobankrs10947223
1000 genomesrs10947223
hgdprs10947223
ensemblrs10947223
gopubmedrs10947223
geneviewrs10947223
scholarrs10947223
googlers10947223
pharmgkbrs10947223
gwascentralrs10947223
openSNPrs10947223
23andMers10947223
23andMe allrs10947223
SNPshotrs10947223
SNPdbers10947223
MSV3drs10947223
GWAS Ctlgrs10947223
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 29283494] Genetic association of complement component 2 variants with chronic hepatitis B in a Korean population.