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rs2121070

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2121070(C;T)
Make rs2121070(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position76184421
GeneGPATCH2L
is asnp
is mentioned by
dbSNPrs2121070
ebirs2121070
HLIrs2121070
Exacrs2121070
Varsomers2121070
Maprs2121070
PheGenIrs2121070
hapmaprs2121070
1000 genomesrs2121070
hgdprs2121070
ensemblrs2121070
gopubmedrs2121070
geneviewrs2121070
scholarrs2121070
googlers2121070
pharmgkbrs2121070
gwascentralrs2121070
openSNPrs2121070
23andMers2121070
23andMe allrs2121070
SNP Nexus

SNPshotrs2121070
SNPdbers2121070
MSV3drs2121070
GWAS Ctlgrs2121070
GMAF0.2268
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903302OA-icon.png]
Trait Blood pressure
Title Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
Risk Allele
P-val 0.0000050000000000000004
Odds Ratio NR NR

[PMID 17903302OA-icon.png] diastolic blood pressure


GET Evidence
rs2121070
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.6875
summary