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rs863223655

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223655(C;T)
Make rs863223655(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10644977
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223655
ebirs863223655
HLIrs863223655
Exacrs863223655
Varsomers863223655
Maprs863223655
PheGenIrs863223655
hapmaprs863223655
1000 genomesrs863223655
hgdprs863223655
ensemblrs863223655
gopubmedrs863223655
geneviewrs863223655
scholarrs863223655
googlers863223655
pharmgkbrs863223655
gwascentralrs863223655
openSNPrs863223655
23andMers863223655
23andMe allrs863223655
SNP Nexus

SNPshotrs863223655
SNPdbers863223655
MSV3drs863223655
GWAS Ctlgrs863223655
Max Magnitude0
ClinVar
Risk rs863223655(T;T)
Alt rs863223655(T;T)
Reference rs863223655(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10625625G>A
CLNSRC
CLNACC RCV000196949.1,