List of variants in gene GFPT1 reported as benign for not provided

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.543+285T>C	rs6724567	0.67625
NM_001244710.2(GFPT1):c.7+239T>C	rs6738707	0.67430
NM_001244710.2(GFPT1):c.7+271A>G	rs6725340	0.66354
NM_001244710.2(GFPT1):c.1010-142A>G	rs4546050	0.66279
NM_001244710.2(GFPT1):c.408+107T>G	rs6546505	0.65886
NM_001244710.2(GFPT1):c.605+206C>T	rs7579871	0.64811
NM_001244710.2(GFPT1):c.7+36T>C	rs6720415	0.57447
NM_001244710.2(GFPT1):c.544-207T>C	rs13389936	0.48926
NM_001244710.2(GFPT1):c.8-257C>T	rs10203394	0.38544
NM_001244710.2(GFPT1):c.1325-158A>G	rs10164798	0.36900
NM_001244710.2(GFPT1):c.2056-293T>G	rs67218758	0.13968
NM_001244710.2(GFPT1):c.1725+285T>G	rs55885494	0.12911
NM_001244710.2(GFPT1):c.1726-263G>A	rs1004137251	0.06980
NM_001244710.2(GFPT1):c.544-183G>A	rs76252573	0.03483
NM_001244710.2(GFPT1):c.409-315G>T	rs116751403	0.02913
NM_001244710.2(GFPT1):c.408+97G>A	rs73937257	0.02428
NM_001244710.2(GFPT1):c.408+7A>T	rs112682152	0.01229
NM_001244710.2(GFPT1):c.1204-146del	rs11296709
NM_001244710.2(GFPT1):c.1204-253_1204-251dup	rs58220809
NM_001244710.2(GFPT1):c.1324+121G>C	rs79296658
NM_001244710.2(GFPT1):c.1324+13del	rs113734896
NM_001244710.2(GFPT1):c.1597+125G>A	rs72905158
NM_001244710.2(GFPT1):c.1726-280_1726-278dup	rs10634143
NM_001244710.2(GFPT1):c.1726-280dup	rs10634143
NM_001244710.2(GFPT1):c.2056-11del	rs201268947
NM_001244710.2(GFPT1):c.2056-12_2056-11del	rs201268947
NM_001244710.2(GFPT1):c.408+30T>C	rs67760762
NM_001244710.2(GFPT1):c.544-185del	rs67434964
NM_001244710.2(GFPT1):c.606-157dup	rs61401084
NM_001244710.2(GFPT1):c.8-218dup	rs5831970

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