Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12811512
rs12811512
Entrez Id: 9052
Gene Symbol: GPRC5A
GPRC5A
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1148732
rs1148732
Entrez Id: 9052;693199
Gene Symbol: GPRC5A;MIR614
GPRC5A;MIR614
CUI: C0153536
Disease:
Malignant melanoma of skin of lower limb
0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480 2018
dbSNP: rs1148732
rs1148732
Entrez Id: 9052;693199
Gene Symbol: GPRC5A;MIR614
GPRC5A;MIR614
CUI: C0151779
Disease:
Cutaneous Melanoma
0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480 2018
dbSNP: rs1148732
rs1148732
Entrez Id: 9052;693199
Gene Symbol: GPRC5A;MIR614
GPRC5A;MIR614
CUI: C0153535
Disease:
Malignant melanoma of skin of upper limb
0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480 2018
dbSNP: rs1640875
rs1640875
Entrez Id: 9052
Gene Symbol: GPRC5A
GPRC5A
CUI: C0153536
Disease:
Malignant melanoma of skin of lower limb
0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480 2018
dbSNP: rs1640875
rs1640875
Entrez Id: 9052
Gene Symbol: GPRC5A
GPRC5A
CUI: C0153535
Disease:
Malignant melanoma of skin of upper limb
0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480 2018
dbSNP: rs1640875
rs1640875
Entrez Id: 9052
Gene Symbol: GPRC5A
GPRC5A
CUI: C0151779
Disease:
Cutaneous Melanoma
0.700 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480 2018
dbSNP: rs12811512
rs12811512
Entrez Id: 9052
Gene Symbol: GPRC5A
GPRC5A
CUI: C0518015
Disease:
Hemoglobin measurement
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs12811512
rs12811512
Entrez Id: 9052
Gene Symbol: GPRC5A
GPRC5A
CUI: C0018935
Disease:
Hematocrit procedure
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs748582997
rs748582997
Entrez Id: 9052
Gene Symbol: GPRC5A
GPRC5A
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder)
0.010 GeneticVariation BEFREE All LUADs were found to harbor somatic mutations in the Kras oncogene (p. G12D or p. Q61R). 28653505 2017
dbSNP: rs773168418
rs773168418
Entrez Id: 9052
Gene Symbol: GPRC5A
GPRC5A
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder)
0.010 GeneticVariation BEFREE All LUADs were found to harbor somatic mutations in the Kras oncogene (p. G12D or p. Q61R). 28653505 2017