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rs587776820

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGGACACCC;AGGACACCC) 0 common in clinvar
(GGTGTCCT;GGTGTCCT) 0 common in clinvar
Make rs587776820(-;-)
Make rs587776820(-;GGTGTCCT)
ReferenceGRCh38 38.1/142
Chromosome19
Position7142871
GeneINSR
is asnp
is mentioned by
dbSNPrs587776820
ebirs587776820
HLIrs587776820
Exacrs587776820
Varsomers587776820
Maprs587776820
PheGenIrs587776820
hapmaprs587776820
1000 genomesrs587776820
hgdprs587776820
ensemblrs587776820
gopubmedrs587776820
geneviewrs587776820
scholarrs587776820
googlers587776820
pharmgkbrs587776820
gwascentralrs587776820
openSNPrs587776820
23andMers587776820
23andMe allrs587776820
SNP Nexus

SNPshotrs587776820
SNPdbers587776820
MSV3drs587776820
GWAS Ctlgrs587776820
Max Magnitude0
ClinVar
Risk rs587776820(GGTGTCCTC,C;GGTGTCCTC,C)
Alt rs587776820(GGTGTCCTC,C;GGTGTCCTC,C)
Reference rs587776820(AGGACACCC;AGGACACCC)
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.7142882_7142889delGGTGTCCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000015828.29,