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rs75326924

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs75326924(C;T)
Make rs75326924(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position80656687
GeneCD36
is asnp
is mentioned by
dbSNPrs75326924
ebirs75326924
HLIrs75326924
Exacrs75326924
Varsomers75326924
Maprs75326924
PheGenIrs75326924
hapmaprs75326924
1000 genomesrs75326924
hgdprs75326924
ensemblrs75326924
gopubmedrs75326924
geneviewrs75326924
scholarrs75326924
googlers75326924
pharmgkbrs75326924
gwascentralrs75326924
openSNPrs75326924
23andMers75326924
23andMe allrs75326924
SNP Nexus

SNPshotrs75326924
SNPdbers75326924
MSV3drs75326924
GWAS Ctlgrs75326924
Merged fromRs3765187
GMAF0.003214
Max Magnitude0
OMIM173510
Desc
Variant0001
Relatedalso
ClinVar
Risk rs75326924(T;T)
Alt rs75326924(T;T)
Reference rs75326924(C;C)
Significance Pathogenic
Disease Platelet glycoprotein IV deficiency
Variation info
Gene CD36
CLNDBN Platelet glycoprotein IV deficiency
Reversed 0
HGVS NC_000007.13:g.80286003C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014490.19,