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rs34377097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34377097(G;T)
Make rs34377097(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position3600456
GeneTBXA2R
is asnp
is mentioned by
dbSNPrs34377097
ebirs34377097
HLIrs34377097
Exacrs34377097
Varsomers34377097
Maprs34377097
PheGenIrs34377097
hapmaprs34377097
1000 genomesrs34377097
hgdprs34377097
ensemblrs34377097
gopubmedrs34377097
geneviewrs34377097
scholarrs34377097
googlers34377097
pharmgkbrs34377097
gwascentralrs34377097
openSNPrs34377097
23andMers34377097
23andMe allrs34377097
SNP Nexus

SNPshotrs34377097
SNPdbers34377097
MSV3drs34377097
GWAS Ctlgrs34377097
GMAF0.0009183
Max Magnitude0
OMIM188070
Desc
Variant0001
Relatedalso


ClinVar
Risk rs34377097(T;T)
Alt rs34377097(T;T)
Reference rs34377097(G;G)
Significance Other
Disease Platelet-type bleeding disorder 13
Variation info
Gene TBXA2R
CLNDBN Platelet-type bleeding disorder 13, susceptibility to
Reversed 1
HGVS NC_000019.9:g.3600454C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013549.2,