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rs863223923

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223923(A;A)
Make rs863223923(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position100990461
GeneC10orf2
is asnp
is mentioned by
dbSNPrs863223923
ebirs863223923
HLIrs863223923
Exacrs863223923
Varsomers863223923
Maprs863223923
PheGenIrs863223923
hapmaprs863223923
1000 genomesrs863223923
hgdprs863223923
ensemblrs863223923
gopubmedrs863223923
geneviewrs863223923
scholarrs863223923
googlers863223923
pharmgkbrs863223923
gwascentralrs863223923
openSNPrs863223923
23andMers863223923
23andMe allrs863223923
SNP Nexus

SNPshotrs863223923
SNPdbers863223923
MSV3drs863223923
GWAS Ctlgrs863223923
Max Magnitude0
ClinVar
Risk rs863223923(A;A)
Alt rs863223923(A;A)
Reference rs863223923(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C10orf2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102750218G>A
CLNSRC
CLNACC RCV000199758.1,