List of variants in gene GAN reported as benign by GeneDx

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_022041.3(GAN):c.-323G>T	rs12599564	0.90188
NM_022041.4(GAN):c.974-303C>T	rs2608552	0.89697
NM_022041.4(GAN):c.1236+256T>C	rs9935709	0.66150
NM_022041.4(GAN):c.1237-59G>A	rs4889313	0.64331
NM_022041.4(GAN):c.*247G>A	rs2216769	0.57491
NM_022041.4(GAN):c.283-283A>G	rs729181	0.47758
NM_022041.4(GAN):c.282+223C>T	rs9938148	0.41322
NM_022041.4(GAN):c.1502+222G>A	rs2615701	0.23571
NM_022041.4(GAN):c.1087-233T>C	rs2550738	0.21940
NM_022041.4(GAN):c.1293C>T (p.Tyr431=)	rs2608555	0.21090
NM_022041.4(GAN):c.1087-161T>C	rs9933250	0.20409
NM_022041.4(GAN):c.1086+71C>T	rs12448327	0.18756
NM_022041.4(GAN):c.1237-261G>A	rs9930065	0.16266
NM_022041.4(GAN):c.*235T>C	rs16955203	0.09343
NM_022041.4(GAN):c.*227G>A	rs113970605	0.05772
NM_022041.4(GAN):c.1503-320A>G	rs73602865	0.05136
NM_022041.4(GAN):c.168-147A>G	rs16955109	0.04225
NM_022041.4(GAN):c.*294A>G	rs16955210	0.04160
NM_022041.4(GAN):c.851+125T>C	rs113656513	0.04087
NM_022041.4(GAN):c.168-66G>A	rs9935105	0.03562
NM_022041.4(GAN):c.*81T>C	rs78835723	0.03196
NM_022041.4(GAN):c.*237T>A	rs113064319	0.02517
NM_022041.4(GAN):c.634-51T>C	rs56859781	0.02138
NM_022041.4(GAN):c.973+148G>A	rs7191388	0.02105
NM_022041.4(GAN):c.1087-225T>A	rs112859650	0.02102
NM_022041.4(GAN):c.1612+13C>G	rs80326128	0.00917
NM_022041.4(GAN):c.168-48C>G	rs77078389	0.00604
NM_022041.4(GAN):c.1239C>T (p.Ile413=)	rs61740238	0.00561
NM_022041.4(GAN):c.1182C>T (p.Tyr394=)	rs150102659	0.00326
NM_022041.4(GAN):c.1086+51C>T	rs78861333
NM_022041.4(GAN):c.1087-314dup	rs35727292
NM_022041.4(GAN):c.283-149del	rs5818329
NM_022041.4(GAN):c.974-186A>G	rs8055288

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