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rs587776819

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776819(C;C)
Make rs587776819(C;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position7172436
GeneINSR
is asnp
is mentioned by
dbSNPrs587776819
ebirs587776819
HLIrs587776819
Exacrs587776819
Varsomers587776819
Maprs587776819
PheGenIrs587776819
hapmaprs587776819
1000 genomesrs587776819
hgdprs587776819
ensemblrs587776819
gopubmedrs587776819
geneviewrs587776819
scholarrs587776819
googlers587776819
pharmgkbrs587776819
gwascentralrs587776819
openSNPrs587776819
23andMers587776819
23andMe allrs587776819
SNP Nexus

SNPshotrs587776819
SNPdbers587776819
MSV3drs587776819
GWAS Ctlgrs587776819
Max Magnitude0
ClinVar
Risk rs587776819(C,T;C,T)
Alt rs587776819(C,T;C,T)
Reference rs587776819(A;A)
Significance Pathogenic
Disease Pineal hyperplasia AND diabetes mellitus syndrome
Variation info
Gene INSR
CLNDBN Pineal hyperplasia AND diabetes mellitus syndrome
Reversed 1
HGVS NC_000019.9:g.7172447T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015827.28,