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rs863223675

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223675(-;-)
Make rs863223675(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10641213
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223675
dbSNP (classic)rs863223675
ClinGenrs863223675
ebirs863223675
HLIrs863223675
Exacrs863223675
Gnomadrs863223675
Varsomers863223675
LitVarrs863223675
Maprs863223675
PheGenIrs863223675
Biobankrs863223675
1000 genomesrs863223675
hgdprs863223675
ensemblrs863223675
geneviewrs863223675
scholarrs863223675
googlers863223675
pharmgkbrs863223675
gwascentralrs863223675
openSNPrs863223675
23andMers863223675
SNPshotrs863223675
SNPdbers863223675
MSV3drs863223675
GWAS Ctlgrs863223675
Max Magnitude0
ClinVar
Risk rs863223675(-;-)
Alt rs863223675(-;-)
Reference Rs863223675(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10621861delA
CLNSRC
CLNACC RCV000196035.1,