Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057524917
rs1057524917
Entrez Id: 83999
Gene Symbol: KREMEN1
KREMEN1
CUI: C4479322
Disease:
ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE 		C 0.800 CausalMutation CLINVAR
dbSNP: rs1057524917
rs1057524917
Entrez Id: 83999
Gene Symbol: KREMEN1
KREMEN1
CUI: C4479322
Disease:
ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE 		0.800 GeneticVariation UNIPROT
dbSNP: rs134594
rs134594
Entrez Id: 25770;83999
Gene Symbol: C22orf31;KREMEN1
C22orf31;KREMEN1
CUI: C0005612
Disease:
Birth Weight 		C 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs33958791
rs33958791
Entrez Id: 83999
Gene Symbol: KREMEN1
KREMEN1
CUI: C0040420
Disease:
Tonometry 		G 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998 2018
dbSNP: rs77320622
rs77320622
Entrez Id: 83999
Gene Symbol: KREMEN1
KREMEN1
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs132289
rs132289
Entrez Id: 83999
Gene Symbol: KREMEN1
KREMEN1
CUI: C0678222
Disease:
Breast Carcinoma 		G 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs134594
rs134594
Entrez Id: 25770;83999
Gene Symbol: C22orf31;KREMEN1
C22orf31;KREMEN1
CUI: C0005612
Disease:
Birth Weight 		C 0.700 GeneticVariation GWASCAT Genome-wide associations for birth weight and correlations with adult disease. 27680694 2016