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rs7557529

From SNPedia

Orientationplus
Stabilizedplus
Make rs7557529(C;C)
Make rs7557529(C;T)
Make rs7557529(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position177270369
is asnp
is mentioned by
dbSNPrs7557529
ebirs7557529
HLIrs7557529
Exacrs7557529
Varsomers7557529
Maprs7557529
PheGenIrs7557529
hapmaprs7557529
1000 genomesrs7557529
hgdprs7557529
ensemblrs7557529
gopubmedrs7557529
geneviewrs7557529
scholarrs7557529
googlers7557529
pharmgkbrs7557529
gwascentralrs7557529
openSNPrs7557529
23andMers7557529
23andMe allrs7557529
SNP Nexus

SNPshotrs7557529
SNPdbers7557529
MSV3drs7557529
GWAS Ctlgrs7557529
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 25496089OA-icon.png] Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson¿s disease ¿ a multicenter study