List of variants reported as benign for Diabetes insipidus, nephrogenic, autosomal

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000486.6(AQP2):c.*1562T>C	rs296766	0.91514
NM_000486.6(AQP2):c.*2495A>G	rs296768	0.91375
NM_000486.6(AQP2):c.607-92A>G	rs410837	0.88050
NM_000486.6(AQP2):c.607-253T>C	rs439779	0.70786
NM_000486.6(AQP2):c.501T>C (p.Ser167=)	rs426496	0.70780
NM_000486.6(AQP2):c.607-39C>G	rs403201	0.70732
NM_000486.6(AQP2):c.*20C>A	rs457487	0.57803
NM_000486.6(AQP2):c.*374C>T	rs467323	0.53117
NM_000486.6(AQP2):c.*1684T>C	rs10875989	0.33771
NM_000486.6(AQP2):c.*2725A>C	rs1077520	0.21838
NM_000486.6(AQP2):c.*3002G>C	rs2878771	0.17599
NM_000486.6(AQP2):c.360+3G>A	rs3741559	0.16237
NM_000486.6(AQP2):c.*3168T>C	rs2878772	0.13262
NM_000486.6(AQP2):c.526-54T>C	rs12372344	0.13174
NM_000486.6(AQP2):c.*1757A>G	rs74091162	0.12242
NM_000486.6(AQP2):c.*1228T>G	rs77904078	0.03005
NM_000486.6(AQP2):c.*2250C>T	rs296767	0.02919
NM_000486.6(AQP2):c.*1395C>T	rs140054228	0.01496
NM_000486.6(AQP2):c.*907C>T	rs60887132	0.01480
NM_000486.6(AQP2):c.342G>A (p.Gly114=)	rs35400945	0.01305
NM_000486.6(AQP2):c.345C>T (p.Asp115=)	rs60629501	0.01171
NM_000486.6(AQP2):c.*2101C>T	rs77661963	0.00919
NM_000486.6(AQP2):c.-59G>A	rs62620006	0.00748
NM_000486.6(AQP2):c.*252G>A	rs114099597	0.00640
NM_000486.6(AQP2):c.*530C>T	rs74091160	0.00589
NM_000486.6(AQP2):c.*1001G>A	rs148904180	0.00559
NM_000486.6(AQP2):c.39G>A (p.Val13=)	rs61733029	0.00540
NM_000486.6(AQP2):c.204C>T (p.Asn68=)	rs57915981	0.00332
NM_000486.6(AQP2):c.*2795T>G	rs1077521	0.00264
NM_000486.6(AQP2):c.*1218T>C	rs376984675	0.00005
NM_000486.6(AQP2):c.438C>T (p.Phe146=)	rs143886391	0.00002
NM_000486.6(AQP2):c.*121C>G	rs75528468
NM_000486.6(AQP2):c.607-59C>A	rs371777

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