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rs797045624

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045624(C;C)
Make rs797045624(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position7167966
GeneINSR
is asnp
is mentioned by
dbSNPrs797045624
ebirs797045624
HLIrs797045624
Exacrs797045624
Varsomers797045624
Maprs797045624
PheGenIrs797045624
hapmaprs797045624
1000 genomesrs797045624
hgdprs797045624
ensemblrs797045624
gopubmedrs797045624
geneviewrs797045624
scholarrs797045624
googlers797045624
pharmgkbrs797045624
gwascentralrs797045624
openSNPrs797045624
23andMers797045624
23andMe allrs797045624
SNP Nexus

SNPshotrs797045624
SNPdbers797045624
MSV3drs797045624
GWAS Ctlgrs797045624
Max Magnitude0
ClinVar
Risk rs797045624(C;C)
Alt rs797045624(C;C)
Reference rs797045624(T;T)
Significance Pathogenic
Disease Hyperinsulinemic hypoglycemia familial 5
Variation info
Gene INSR
CLNDBN Hyperinsulinemic hypoglycemia familial 5
Reversed 1
HGVS NC_000019.9:g.7167977A>G
CLNSRC
CLNACC RCV000194300.1,