List of variants in gene GFPT1 reported as benign by Illumina Laboratory Services, Illumina

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001244710.2(GFPT1):c.*3065G>A	rs7568296	0.67342
NM_001244710.2(GFPT1):c.*5001G>A	rs13396883	0.66919
NM_001244710.2(GFPT1):c.*3285A>G	rs7579532	0.66906
NM_001244710.2(GFPT1):c.*6085C>G	rs7642	0.66555
NM_001244710.2(GFPT1):c.*2269A>G	rs10198171	0.66442
NM_001244710.2(GFPT1):c.*4059A>G	rs13751	0.65899
NM_001244710.2(GFPT1):c.1105+7A>G	rs6722492	0.65895
NM_001244710.2(GFPT1):c.*3091A>C	rs7582334	0.65873
NM_001244710.2(GFPT1):c.*2669C>T	rs10185336	0.65232
NM_001244710.2(GFPT1):c.*800G>T	rs2667	0.65228
NM_001244710.2(GFPT1):c.*2310A>G	rs10198150	0.65225
NM_001244710.2(GFPT1):c.*4730G>A	rs28694003	0.65218
NM_001244710.2(GFPT1):c.*4826A>C	rs67016706	0.12917
NM_001244710.2(GFPT1):c.*1244G>T	rs73937246	0.02428
NM_001244710.2(GFPT1):c.*6094C>T	rs55888680	0.02423
NM_001244710.2(GFPT1):c.147T>C (p.Asp49=)	rs2230300	0.01692
NM_001244710.2(GFPT1):c.*2685A>G	rs74972420	0.01293
NM_001244710.2(GFPT1):c.*2219C>T	rs149217357	0.01291
NM_001244710.2(GFPT1):c.408+7A>T	rs112682152	0.01229
NM_001244710.2(GFPT1):c.*603G>A	rs78097440	0.01222
NM_001244710.2(GFPT1):c.*1085A>G	rs75177078	0.01153
NM_001244710.2(GFPT1):c.*4053T>A	rs4128250	0.01067
NM_001244710.2(GFPT1):c.675C>T (p.Leu225=)	rs78952091	0.00975
NM_001244710.2(GFPT1):c.*4403G>T	rs148687340	0.00642
NM_001244710.2(GFPT1):c.*6366T>C	rs115964031	0.00633
NM_001244710.2(GFPT1):c.*2511T>A	rs60949141	0.00572
NM_001244710.2(GFPT1):c.*3781G>T	rs116952694	0.00177
NM_001244710.2(GFPT1):c.*2907C>T	rs7568674
NM_001244710.2(GFPT1):c.*3345C>T	rs73937245
NM_001244710.2(GFPT1):c.*870C>A	rs77753566

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