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rs863223664

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs863223664(GC;T)
Make rs863223664(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10658574
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223664
dbSNP (classic)rs863223664
ClinGenrs863223664
ebirs863223664
HLIrs863223664
Exacrs863223664
Gnomadrs863223664
Varsomers863223664
LitVarrs863223664
Maprs863223664
PheGenIrs863223664
Biobankrs863223664
1000 genomesrs863223664
hgdprs863223664
ensemblrs863223664
geneviewrs863223664
scholarrs863223664
googlers863223664
pharmgkbrs863223664
gwascentralrs863223664
openSNPrs863223664
23andMers863223664
SNPshotrs863223664
SNPdbers863223664
MSV3drs863223664
GWAS Ctlgrs863223664
Max Magnitude0
ClinVar
Risk rs863223664(T;T)
Alt rs863223664(T;T)
Reference Rs863223664(GC;GC)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10639222_10639223delGCinsA
CLNSRC
CLNACC RCV000198520.1,