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rs863223922

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223922(A;A)
Make rs863223922(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position100989706
GeneC10orf2
is asnp
is mentioned by
dbSNPrs863223922
ebirs863223922
HLIrs863223922
Exacrs863223922
Varsomers863223922
Maprs863223922
PheGenIrs863223922
hapmaprs863223922
1000 genomesrs863223922
hgdprs863223922
ensemblrs863223922
gopubmedrs863223922
geneviewrs863223922
scholarrs863223922
googlers863223922
pharmgkbrs863223922
gwascentralrs863223922
openSNPrs863223922
23andMers863223922
23andMe allrs863223922
SNP Nexus

SNPshotrs863223922
SNPdbers863223922
MSV3drs863223922
GWAS Ctlgrs863223922
Max Magnitude0
ClinVar
Risk rs863223922(A;A)
Alt rs863223922(A;A)
Reference rs863223922(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene C10orf2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102749463G>A
CLNSRC
CLNACC RCV000197887.1,