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rs33958176

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs33958176(A;A)
Make rs33958176(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position98911384
GeneIGF1R
is asnp
is mentioned by
dbSNPrs33958176
dbSNP (classic)rs33958176
ClinGenrs33958176
ebirs33958176
HLIrs33958176
Exacrs33958176
Gnomadrs33958176
Varsomers33958176
LitVarrs33958176
Maprs33958176
PheGenIrs33958176
Biobankrs33958176
1000 genomesrs33958176
hgdprs33958176
ensemblrs33958176
geneviewrs33958176
scholarrs33958176
googlers33958176
pharmgkbrs33958176
gwascentralrs33958176
openSNPrs33958176
23andMers33958176
SNPshotrs33958176
SNPdbers33958176
MSV3drs33958176
GWAS Ctlgrs33958176
GMAF0.0009183
Max Magnitude0
OMIM147370
Desc
Variant0005
Relatedalso
ClinVar
Risk rs33958176(A;A)
Alt rs33958176(A;A)
Reference Rs33958176(G;G)
Significance Other
Disease Insulin-like growth factor 1 resistance to not specified not provided
Variation info
Gene IGF1R
CLNDBN Insulin-like growth factor 1 resistance to not specified not provided
Reversed 0
HGVS NC_000015.9:g.99454613G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000015917.26, RCV000369272.1, RCV000487894.1,


[PMID 20625407OA-icon.png] A comprehensive in silico analysis of the functional and structural impact of SNPs in the IGF1R gene.