List of variants in gene TMPO reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001032283.3(TMPO):c.565+2214C>G	rs17459334	0.06758
NM_001032283.3(TMPO):c.565+1369C>G	rs35969221	0.03471
NM_001032283.3(TMPO):c.565+1665A>G	rs11838270	0.02179
NM_001032283.3(TMPO):c.991-4T>C	rs112475937	0.01905
NM_001032283.3(TMPO):c.565+1296T>G	rs35645287	0.01895
NM_001032283.3(TMPO):c.565+1132T>G	rs35998138	0.01742
NM_001032283.3(TMPO):c.565+1853G>C	rs35761089	0.01735
NM_001032283.3(TMPO):c.565+2051T>A	rs12316677	0.01280
NM_001032283.3(TMPO):c.565+1890T>G	rs80325832	0.01253
NM_001032283.3(TMPO):c.565+1344G>C	rs114939776	0.01252
NM_001032283.3(TMPO):c.859G>C (p.Ala287Pro)	rs7133258	0.00977
NM_001032283.3(TMPO):c.565+2487C>T	rs17028450	0.00576
NM_001032283.3(TMPO):c.87C>T (p.Ala29=)	rs114074541	0.00153
NM_001032283.3(TMPO):c.565+1105C>T	rs138790561	0.00038
NM_001032283.3(TMPO):c.1079+5dup	rs34449077

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