List of variants in gene ARHGAP32 reported as likely benign for ARHGAP32-related disorder

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_001378024.1(ARHGAP32):c.2175A>G (p.Thr725=)	rs61753088	0.00452
NM_001378024.1(ARHGAP32):c.5832C>T (p.Ser1944=)	rs78689455	0.00139
NM_001378024.1(ARHGAP32):c.6172G>A (p.Gly2058Ser)	rs112106627	0.00131
NM_001378024.1(ARHGAP32):c.3659G>A (p.Arg1220His)	rs139276969	0.00111
NM_001378024.1(ARHGAP32):c.4206C>T (p.Asp1402=)	rs144145037	0.00084
NM_001378024.1(ARHGAP32):c.3105C>T (p.Ser1035=)	rs143245403	0.00078
NM_001378024.1(ARHGAP32):c.1299C>T (p.Arg433=)	rs142881922	0.00064
NM_001378024.1(ARHGAP32):c.4887A>G (p.Arg1629=)	rs146744767	0.00057
NM_001378024.1(ARHGAP32):c.5082C>T (p.Pro1694=)	rs183293077	0.00032
NM_001378024.1(ARHGAP32):c.2124T>C (p.Gly708=)	rs146345062	0.00016
NM_001378024.1(ARHGAP32):c.3270G>A (p.Ala1090=)	rs141213420	0.00013
NM_001378024.1(ARHGAP32):c.445-5T>C	rs368394867	0.00012
NM_001378024.1(ARHGAP32):c.4812G>A (p.Pro1604=)	rs567546669	0.00006
NM_001378024.1(ARHGAP32):c.1098T>C (p.Ser366=)	rs535110024	0.00005
NM_001378024.1(ARHGAP32):c.1299-7A>G
NM_001378024.1(ARHGAP32):c.5982C>A (p.Pro1994=)	rs139852631
NM_001378024.1(ARHGAP32):c.6300A>G (p.Ala2100=)	rs147546090

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