Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223671

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
(D;D) 0 common genotype
Make rs863223671(-;C)
Make rs863223671(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10650275
GeneJAG1, MIR6870
is asnp
is mentioned by
dbSNPrs863223671
dbSNP (classic)rs863223671
ClinGenrs863223671
ebirs863223671
HLIrs863223671
Exacrs863223671
Gnomadrs863223671
Varsomers863223671
LitVarrs863223671
Maprs863223671
PheGenIrs863223671
Biobankrs863223671
1000 genomesrs863223671
hgdprs863223671
ensemblrs863223671
geneviewrs863223671
scholarrs863223671
googlers863223671
pharmgkbrs863223671
gwascentralrs863223671
openSNPrs863223671
23andMers863223671
SNPshotrs863223671
SNPdbers863223671
MSV3drs863223671
GWAS Ctlgrs863223671
Max Magnitude0
ClinVar
Risk rs863223671(C;C)
Alt rs863223671(C;C)
Reference Rs863223671(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR6870 JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10630924dupG
CLNSRC
CLNACC RCV000197265.1,