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rs1131695

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1131695(C;T)
Make rs1131695(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10652589
GeneJAG1
is asnp
is mentioned by
dbSNPrs1131695
ebirs1131695
HLIrs1131695
Exacrs1131695
Varsomers1131695
Maprs1131695
PheGenIrs1131695
hapmaprs1131695
1000 genomesrs1131695
hgdprs1131695
ensemblrs1131695
gopubmedrs1131695
geneviewrs1131695
scholarrs1131695
googlers1131695
pharmgkbrs1131695
gwascentralrs1131695
openSNPrs1131695
23andMers1131695
23andMe allrs1131695
SNP Nexus

SNPshotrs1131695
SNPdbers1131695
MSV3drs1131695
GWAS Ctlgrs1131695
Max Magnitude0
ClinVar
Risk rs1131695(A,G,T;A,G,T)
Alt rs1131695(A,G,T;A,G,T)
Reference rs1131695(C;C)
Significance Pathogenic
Disease not specified not provided
Variation info
Gene JAG1
CLNDBN not specified not provided
Reversed 1
HGVS NC_000020.10:g.10633237G\x3d; NC_000020.10:g.10633237G>A; NC_000020.10:g.10633237G>C
CLNSRC
CLNACC RCV000150845.2, RCV000132569.1, RCV000199026.1, RCV000214085.1,