List of variants reported as benign for Amelocerebrohypohidrotic syndrome

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Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_024589.3(ROGDI):c.823-22A>G	rs1982515	0.42702
NM_024589.3(ROGDI):c.*292C>T	rs8118	0.40388
NM_024589.3(ROGDI):c.*144G>A	rs7546	0.40047
NM_024589.3(ROGDI):c.414G>A (p.Thr138=)	rs11553876	0.10521
NM_024589.3(ROGDI):c.822+17C>T	rs111272920	0.02340
NM_024589.3(ROGDI):c.393C>G (p.Asp131Glu)	rs143095485	0.01923
NM_024589.3(ROGDI):c.433-15C>T	rs114103417	0.00806
NM_024589.3(ROGDI):c.696C>T (p.Phe232=)	rs75818610	0.00686
NM_024589.3(ROGDI):c.646-5C>T	rs115660765	0.00647
NM_024589.3(ROGDI):c.*270T>C	rs76192577	0.00642
NM_024589.3(ROGDI):c.713G>A (p.Arg238His)	rs138409264	0.00548
NM_024589.3(ROGDI):c.45+19C>G	rs546936996	0.00397
NM_024589.3(ROGDI):c.522C>T (p.Ser174=)	rs150687774	0.00190
NM_024589.3(ROGDI):c.118-13C>G	rs201794245	0.00137
NM_024589.3(ROGDI):c.783C>T (p.Phe261=)	rs142481526	0.00075
NM_024589.3(ROGDI):c.243C>T (p.Ala81=)	rs148051351	0.00073
NM_024589.3(ROGDI):c.432+13C>T	rs371432203	0.00071
NM_024589.3(ROGDI):c.567G>A (p.Leu189=)	rs143000899	0.00059
NM_024589.3(ROGDI):c.489C>T (p.Pro163=)	rs113245789	0.00056
NM_024589.3(ROGDI):c.532-4G>A	rs3747610	0.00017
NM_024589.3(ROGDI):c.696-8G>T	rs3747609	0.00008
NM_024589.3(ROGDI):c.823-10C>T	rs199642172	0.00007
NM_024589.3(ROGDI):c.417C>T (p.Gly139=)	rs375517608	0.00001
NM_024589.3(ROGDI):c.678T>C (p.His226=)	rs549672547	0.00001
NM_024589.2(ROGDI):c.-320C>G	rs17137286
NM_024589.3(ROGDI):c.117+10C>G	rs113858060
NM_024589.3(ROGDI):c.117+10C>T	rs113858060
NM_024589.3(ROGDI):c.118-24_118-17del	rs145700776
NM_024589.3(ROGDI):c.432+13dup	rs2082693928
NM_024589.3(ROGDI):c.45+37_46-30del	rs786205125
NM_024589.3(ROGDI):c.645+15del	rs1356112429
NM_024589.3(ROGDI):c.786C>G (p.Thr262=)	rs146812127

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