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

rs114202595

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs114202595(A;A)
Make rs114202595(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position127614533
GenePAX4
is asnp
is mentioned by
dbSNPrs114202595
ebirs114202595
HLIrs114202595
Exacrs114202595
Varsomers114202595
Maprs114202595
PheGenIrs114202595
hapmaprs114202595
1000 genomesrs114202595
hgdprs114202595
ensemblrs114202595
gopubmedrs114202595
geneviewrs114202595
scholarrs114202595
googlers114202595
pharmgkbrs114202595
gwascentralrs114202595
openSNPrs114202595
23andMers114202595
23andMe allrs114202595
SNP Nexus

SNPshotrs114202595
SNPdbers114202595
MSV3drs114202595
GWAS Ctlgrs114202595
Merged fromRs121917717
GMAF0.001377
Max Magnitude0
OMIM167413
Desc
Variant0001
Relatedalso
ClinVar
Risk rs114202595(A,T;A,T)
Alt rs114202595(A,T;A,T)
Reference rs114202595(G;G)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene PAX4
CLNDBN Diabetes mellitus type 2
Reversed 0
HGVS NC_000007.13:g.127254587G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014800.25,