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

rs10495098

From SNPedia

Orientationplus
Make rs10495098(G;G)
Make rs10495098(G;T)
Make rs10495098(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position218342968
is asnp
is mentioned by
dbSNPrs10495098
ebirs10495098
HLIrs10495098
Exacrs10495098
Varsomers10495098
Maprs10495098
PheGenIrs10495098
hapmaprs10495098
1000 genomesrs10495098
hgdprs10495098
ensemblrs10495098
gopubmedrs10495098
geneviewrs10495098
scholarrs10495098
googlers10495098
pharmgkbrs10495098
gwascentralrs10495098
openSNPrs10495098
23andMers10495098
23andMe allrs10495098
SNP Nexus

SNPshotrs10495098
SNPdbers10495098
MSV3drs10495098
GWAS Ctlgrs10495098
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 27564654] Genetic variance of transforming growth factor β2 gene in conotruncal heart defects.