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rs774372899

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774372899(C;T)
Make rs774372899(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10643822
GeneJAG1
is asnp
is mentioned by
dbSNPrs774372899
ebirs774372899
HLIrs774372899
Exacrs774372899
Varsomers774372899
Maprs774372899
PheGenIrs774372899
hapmaprs774372899
1000 genomesrs774372899
hgdprs774372899
ensemblrs774372899
gopubmedrs774372899
geneviewrs774372899
scholarrs774372899
googlers774372899
pharmgkbrs774372899
gwascentralrs774372899
openSNPrs774372899
23andMers774372899
23andMe allrs774372899
SNP Nexus

SNPshotrs774372899
SNPdbers774372899
MSV3drs774372899
GWAS Ctlgrs774372899
Max Magnitude0
ClinVar
Risk rs774372899(T;T)
Alt rs774372899(T;T)
Reference rs774372899(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.10624470C>T
CLNSRC
CLNACC RCV000198001.1,