rs16998073

This is a upstream gene variant variant.

GWAS Catalog Trait Associations (28)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

red blood cell density

Allele T
OR 0.03
p 5.0e-39
N 545,203
Large GWAS
European

fibroblast growth factor 5 level

Kalnapenkis A et al. Genetic determinants of plasma protein levels in the Estonian population. Scientific Reports 14(1):7694 (2024)
Allele T
OR 0.59
p 8.0e-34
N 489
Small GWAS
European

aging

Lin WY et al. Lifestyle Factors and Genetic Variants on 2 Biological Age Measures: Evidence From 94 443 Taiwan Biobank Participants. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences 77(6):1189-1198 (2022)
Allele T
OR 0.10
p 6.0e-26
N 25,460
Large GWAS
East Asian

cryptic phenotype measurement

Allele T
OR 0.01
p 5.0e-24
N 308,095
Large GWAS
European

blood protein amount

Allele T
OR 0.50
p 6.0e-22
N 982
Small GWAS
European

preeclampsia, hypertension, pregnancy-induced

Allele T
OR 1.14
p 6.0e-19
N 130,207
Large GWAS
European

hemoglobin measurement

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.02
p 4.0e-17
N 407,887
Major Consortium StudyLarge GWAS
European

hematocrit

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.02
p 8.0e-16
N 407,836
Major Consortium StudyLarge GWAS
European

preeclampsia

Allele T
OR 1.12
p 1.0e-15
N 593,648
Large GWAS
European, Central Asian
Honigberg MC et al. Polygenic prediction of preeclampsia and gestational hypertension. Nature Medicine 29(6):1540-1549 (2023)
Allele T
OR 1.11
p 2.0e-15
N 455,887
Large GWAS
multi-ancestry
Allele T
OR 0.88
p 4.0e-14
N 294,039
Large GWAS
European

pulse pressure measurement

Allele A
OR 0.23
p 1.0e-15
N 321,262
Large GWAS
multi-ancestry
Allele A
OR 0.41
p 2.0e-12
N 130,777
Large GWAS
multi-ancestry

This variant is in our database but has no known associations or PRS memberships yet.

Gene information from NCBI Gene. Variant classifications from ClinVar.

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