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rs397515519

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515519(A;G)
Make rs397515519(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2159793
GeneINS, INS-IGF2
is asnp
is mentioned by
dbSNPrs397515519
ebirs397515519
HLIrs397515519
Exacrs397515519
Varsomers397515519
Maprs397515519
PheGenIrs397515519
hapmaprs397515519
1000 genomesrs397515519
hgdprs397515519
ensemblrs397515519
gopubmedrs397515519
geneviewrs397515519
scholarrs397515519
googlers397515519
pharmgkbrs397515519
gwascentralrs397515519
openSNPrs397515519
23andMers397515519
23andMe allrs397515519
SNP Nexus

SNPshotrs397515519
SNPdbers397515519
MSV3drs397515519
GWAS Ctlgrs397515519
Max Magnitude0
ClinVar
Risk rs397515519(G;G)
Alt rs397515519(G;G)
Reference rs397515519(A;A)
Significance Pathogenic
Disease Permanent neonatal diabetes mellitus
Variation info
Gene INS IGF2 INS-IGF2
CLNDBN Permanent neonatal diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.2181023T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000055785.1,