{{Rsnum
|rsid=34377097
|Gene=TBXA2R
|Chromosome=19
|position=3600456
|Orientation=minus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=TBXA2R
}}{{omim
|id=188070
|rsnum=34377097
|variant=0001
}}

{{ClinVar
|rsid=34377097
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=3600454
|CHROM=19
|GMAF=0.0009
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050160000000000116110100
|GENEINFO=TBXA2R:6915
|GENE_NAME=TBXA2R
|GENE_ID=6915
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.3600454C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=188070.0001
|CLNSIG=255
|CLNCUI=CN078924
|CLNDBN=Platelet-type bleeding disorder 13, susceptibility to
|Disease=Platelet-type bleeding disorder 13
|CLNACC=RCV000013549.1
|Tags=RV;PM;SLO;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3279614:614009
|COMMON=0
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}