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

rs193929357

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193929357(A;A)
Make rs193929357(A;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17387095
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs193929357
dbSNP (classic)rs193929357
ClinGenrs193929357
ebirs193929357
HLIrs193929357
Exacrs193929357
Gnomadrs193929357
Varsomers193929357
LitVarrs193929357
Maprs193929357
PheGenIrs193929357
Biobankrs193929357
1000 genomesrs193929357
hgdprs193929357
ensemblrs193929357
geneviewrs193929357
scholarrs193929357
googlers193929357
pharmgkbrs193929357
gwascentralrs193929357
openSNPrs193929357
23andMers193929357
SNPshotrs193929357
SNPdbers193929357
MSV3drs193929357
GWAS Ctlgrs193929357
Max Magnitude0
ClinVar
Risk rs193929357(A;A)
Alt rs193929357(A;A)
Reference Rs193929357(T;T)
Significance Pathogenic
Disease Permanent neonatal diabetes mellitus
Variation info
Gene KCNJ11
CLNDBN Permanent neonatal diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17408642A>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020362.1,