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rs863223926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223926(-;ATCC)
Make rs863223926(ATCC;ATCC)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position123253773
GeneC12orf65, LOC105370040
is asnp
is mentioned by
dbSNPrs863223926
ClinGenrs863223926
ebirs863223926
HLIrs863223926
Exacrs863223926
Varsomers863223926
Maprs863223926
PheGenIrs863223926
hapmaprs863223926
1000 genomesrs863223926
hgdprs863223926
ensemblrs863223926
gopubmedrs863223926
geneviewrs863223926
scholarrs863223926
googlers863223926
pharmgkbrs863223926
gwascentralrs863223926
openSNPrs863223926
23andMers863223926
23andMe allrs863223926
SNP Nexus

SNPshotrs863223926
SNPdbers863223926
MSV3drs863223926
GWAS Ctlgrs863223926
Max Magnitude0
ClinVar
Risk rs863223926(ATCC;ATCC)
Alt rs863223926(ATCC;ATCC)
Reference Rs863223926(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene C12orf65
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.123738317_123738320dupATCC
CLNSRC
CLNACC RCV000198209.1,