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rs17619601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17619601(C;T)
Make rs17619601(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position28326373
GeneFLT1
is asnp
is mentioned by
dbSNPrs17619601
ebirs17619601
HLIrs17619601
Exacrs17619601
Varsomers17619601
Maprs17619601
PheGenIrs17619601
hapmaprs17619601
1000 genomesrs17619601
hgdprs17619601
ensemblrs17619601
gopubmedrs17619601
geneviewrs17619601
scholarrs17619601
googlers17619601
pharmgkbrs17619601
gwascentralrs17619601
openSNPrs17619601
23andMers17619601
23andMe allrs17619601
SNP Nexus

SNPshotrs17619601
SNPdbers17619601
MSV3drs17619601
GWAS Ctlgrs17619601
GMAF0.03306
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 21751195OA-icon.png] Interactions between environmental factors and polymorphisms in angiogenesis pathway genes in esophageal adenocarcinoma risk: a case-only study