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rs863225073

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225073(G;T)
Make rs863225073(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position114325871
GeneCHAMP1
is asnp
is mentioned by
dbSNPrs863225073
ebirs863225073
HLIrs863225073
Exacrs863225073
Varsomers863225073
Maprs863225073
PheGenIrs863225073
hapmaprs863225073
1000 genomesrs863225073
hgdprs863225073
ensemblrs863225073
gopubmedrs863225073
geneviewrs863225073
scholarrs863225073
googlers863225073
pharmgkbrs863225073
gwascentralrs863225073
openSNPrs863225073
23andMers863225073
23andMe allrs863225073
SNP Nexus

SNPshotrs863225073
SNPdbers863225073
MSV3drs863225073
GWAS Ctlgrs863225073
Max Magnitude0
ClinVar
Risk rs863225073(T;T)
Alt rs863225073(T;T)
Reference rs863225073(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHAMP1
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.115091346G>T
CLNSRC
CLNACC RCV000202219.1,