List of variants in gene GAN reported as benign by Invitae

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_022041.4(GAN):c.1293C>T (p.Tyr431=)	rs2608555	0.21491
NM_022041.4(GAN):c.1612+13C>G	rs80326128	0.00917
NM_022041.4(GAN):c.1239C>T (p.Ile413=)	rs61740238	0.00609
NM_022041.4(GAN):c.1684C>G (p.Pro562Ala)	rs79901179	0.00388
NM_022041.4(GAN):c.1182C>T (p.Tyr394=)	rs150102659	0.00357
NM_022041.4(GAN):c.1502+11A>G	rs143413333	0.00263
NM_022041.4(GAN):c.633+19A>G	rs112194888	0.00138
NM_022041.4(GAN):c.1612+12A>G	rs150344737	0.00135
NM_022041.4(GAN):c.1162C>T (p.Leu388=)	rs73589395	0.00103
NM_022041.4(GAN):c.283-20T>C	rs371984923	0.00093
NM_022041.4(GAN):c.974-11G>C	rs753746307	0.00026
NM_022041.4(GAN):c.634-15T>C	rs367608270	0.00013
NM_022041.4(GAN):c.1373+18G>A	rs187260981	0.00006
NM_022041.4(GAN):c.1086+25_1086+28del	rs561109989
NM_022041.4(GAN):c.168-12dup
NM_022041.4(GAN):c.1728G>C (p.Ala576=)	rs150342446
NM_022041.4(GAN):c.282+7_282+9del	rs563977770

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