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

rs6218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs6218(C;C)
Make rs6218(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position102399855
GeneIGF1, LOC105369942
is asnp
is mentioned by
dbSNPrs6218
dbSNP (old)rs6218
ClinGenrs6218
ebirs6218
HLIrs6218
Exacrs6218
Varsomers6218
Maprs6218
PheGenIrs6218
Biobankrs6218
1000 genomesrs6218
hgdprs6218
ensemblrs6218
gopubmedrs6218
geneviewrs6218
scholarrs6218
googlers6218
pharmgkbrs6218
gwascentralrs6218
openSNPrs6218
23andMers6218
23andMe allrs6218
SNP Nexus

SNPshotrs6218
SNPdbers6218
MSV3drs6218
GWAS Ctlgrs6218
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 26068646] The Functional Variant in the 3'UTR of IGF1 with the Risk of Gastric Cancer in a Chinese Population


ClinVar
Risk rs6218(C;C)
Alt rs6218(C;C)
Reference Rs6218(T;T)
Significance Non-pathogenic
Disease Insulin-like growth factor I deficiency
Variation info
Gene IGF1
CLNDBN Insulin-like growth factor I deficiency
Reversed 1
HGVS NC_000012.11:g.102793633A>G
CLNSRC
CLNACC RCV000362408.1,