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

rs121913155

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913155(A;T)
Make rs121913155(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position7267555
GeneINSR
is asnp
is mentioned by
dbSNPrs121913155
ebirs121913155
HLIrs121913155
Exacrs121913155
Varsomers121913155
Maprs121913155
PheGenIrs121913155
hapmaprs121913155
1000 genomesrs121913155
hgdprs121913155
ensemblrs121913155
gopubmedrs121913155
geneviewrs121913155
scholarrs121913155
googlers121913155
pharmgkbrs121913155
gwascentralrs121913155
openSNPrs121913155
23andMers121913155
23andMe allrs121913155
SNP Nexus

SNPshotrs121913155
SNPdbers121913155
MSV3drs121913155
GWAS Ctlgrs121913155
Max Magnitude0
OMIM147670
Desc
Variant0027
Relatedalso
ClinVar
Risk rs121913155(T;T)
Alt rs121913155(T;T)
Reference rs121913155(A;A)
Significance Pathogenic
Disease Leprechaunism syndrome
Variation info
Gene INSR
CLNDBN Leprechaunism syndrome
Reversed 1
HGVS NC_000019.9:g.7267566T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015820.24,