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rs192902098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs192902098(A;A)
Make rs192902098(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position27920235
GenePDX1, PDX1-AS1
is asnp
is mentioned by
dbSNPrs192902098
dbSNP (classic)rs192902098
ClinGenrs192902098
ebirs192902098
HLIrs192902098
Exacrs192902098
Gnomadrs192902098
Varsomers192902098
LitVarrs192902098
Maprs192902098
PheGenIrs192902098
Biobankrs192902098
1000 genomesrs192902098
hgdprs192902098
ensemblrs192902098
geneviewrs192902098
scholarrs192902098
googlers192902098
pharmgkbrs192902098
gwascentralrs192902098
openSNPrs192902098
23andMers192902098
SNPshotrs192902098
SNPdbers192902098
MSV3drs192902098
GWAS Ctlgrs192902098
Max Magnitude0
ClinVar
Risk rs192902098(A;A) rs192902098(G;G) rs192902098(T;T)
Alt rs192902098(A;A) rs192902098(G;G) rs192902098(T;T)
Reference Rs192902098(C;C)
Significance Probable-Pathogenic
Disease Maturity-onset diabetes of the young not provided
Variation info
Gene PDX1-AS1 PDX1
CLNDBN Maturity-onset diabetes of the young, type 4 not provided
Reversed 0
HGVS NC_000013.10:g.28494372C>A
CLNSRC
CLNACC RCV000030086.1, RCV000414508.1,