rs34377097

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs34377097(G;T)

Make rs34377097(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

3600456

Gene

TBXA2R

is a	snp
is	mentioned by
dbSNP	rs34377097
dbSNP (classic)	rs34377097
ClinGen	rs34377097
ebi	rs34377097
HLI	rs34377097
Exac	rs34377097
Gnomad	rs34377097
Varsome	rs34377097
LitVar	rs34377097
Map	rs34377097
PheGenI	rs34377097
Biobank	rs34377097
1000 genomes	rs34377097
hgdp	rs34377097
ensembl	rs34377097
geneview	rs34377097
scholar	rs34377097
google	rs34377097
pharmgkb	rs34377097
gwascentral	rs34377097
openSNP	rs34377097
23andMe	rs34377097
SNPshot	rs34377097
SNPdbe	rs34377097
MSV3d	rs34377097
GWAS Ctlg	rs34377097

GMAF

0.0009183

Max Magnitude

0

OMIM	188070
Desc
Variant	0001
Related	also

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 UniProtKB (protein)
CLNACC	RCV000013549.2,