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rs121918035

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918035(A;C)
Make rs121918035(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position80673392
GeneCD36
is asnp
is mentioned by
dbSNPrs121918035
ebirs121918035
HLIrs121918035
Exacrs121918035
Varsomers121918035
Maprs121918035
PheGenIrs121918035
hapmaprs121918035
1000 genomesrs121918035
hgdprs121918035
ensemblrs121918035
gopubmedrs121918035
geneviewrs121918035
scholarrs121918035
googlers121918035
pharmgkbrs121918035
gwascentralrs121918035
openSNPrs121918035
23andMers121918035
23andMe allrs121918035
SNP Nexus

SNPshotrs121918035
SNPdbers121918035
MSV3drs121918035
GWAS Ctlgrs121918035
Max Magnitude0
OMIM173510
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918035(C;C)
Alt rs121918035(C;C)
Reference rs121918035(A;A)
Significance Pathogenic
Disease Platelet glycoprotein IV deficiency
Variation info
Gene CD36
CLNDBN Platelet glycoprotein IV deficiency
Reversed 0
HGVS NC_000007.13:g.80302708A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014499.25,