|
NM_001046.3(SLC12A2):c.524G>C (p.Gly175Ala)
|
rs149585221
|
0.00499
|
|
NM_001046.3(SLC12A2):c.102G>A (p.Leu34=)
|
rs535757373
|
0.00241
|
|
NM_001046.3(SLC12A2):c.2322A>C (p.Ser774=)
|
rs115357531
|
0.00153
|
|
NM_001046.3(SLC12A2):c.3468A>G (p.Leu1156=)
|
rs115092488
|
0.00098
|
|
NM_001046.3(SLC12A2):c.876+17_876+18del
|
rs556046317
|
0.00094
|
|
NM_001046.3(SLC12A2):c.2748A>T (p.Gly916=)
|
rs141683516
|
0.00080
|
|
NM_001046.3(SLC12A2):c.2005+9T>C
|
rs10463502
|
0.00071
|
|
NM_001046.3(SLC12A2):c.261C>T (p.Ser87=)
|
rs543480974
|
0.00068
|
|
NM_001046.3(SLC12A2):c.3100+13A>T
|
rs199929591
|
0.00066
|
|
NM_001046.3(SLC12A2):c.495C>T (p.Asp165=)
|
rs138234695
|
0.00051
|
|
NM_001046.3(SLC12A2):c.953-7C>T
|
rs201608609
|
0.00044
|
|
NM_001046.3(SLC12A2):c.1941A>G (p.Lys647=)
|
rs190573592
|
0.00030
|
|
NM_001046.3(SLC12A2):c.2493C>A (p.Ala831=)
|
rs138341229
|
0.00026
|
|
NM_001046.3(SLC12A2):c.2511C>T (p.Ile837=)
|
rs1053614
|
0.00019
|
|
NM_001046.3(SLC12A2):c.41G>T (p.Gly14Val)
|
rs1014756958
|
0.00017
|
|
NM_001046.3(SLC12A2):c.1128C>T (p.Asn376=)
|
rs371700719
|
0.00016
|
|
NM_001046.3(SLC12A2):c.235A>C (p.Ser79Arg)
|
rs557916029
|
0.00014
|
|
NM_001046.3(SLC12A2):c.1773+15T>C
|
rs199958255
|
0.00012
|
|
NM_001046.3(SLC12A2):c.788A>C (p.Glu263Ala)
|
rs367694835
|
0.00011
|
|
NM_001046.3(SLC12A2):c.877-16C>G
|
rs530956302
|
0.00008
|
|
NM_001046.3(SLC12A2):c.3100+20T>A
|
rs776147551
|
0.00003
|
|
NM_001046.3(SLC12A2):c.1226T>C (p.Ile409Thr)
|
rs1485381198
|
0.00002
|
|
NM_001046.3(SLC12A2):c.2475+11A>G
|
rs763550873
|
0.00002
|
|
NM_001046.3(SLC12A2):c.2210T>A (p.Leu737Gln)
|
rs376802988
|
0.00001
|
|
NM_001046.3(SLC12A2):c.2293C>G (p.Leu765Val)
|
rs548545596
|
0.00001
|
|
NC_000005.9:g.127441491_127471419delinsATGAAAAGCTTTACAGAAGTTGGAATTAAAAAAA
|
|
|
|
NM_001046.3(SLC12A2):c.1127A>G (p.Asn376Ser)
|
rs116621105
|
|
|
NM_001046.3(SLC12A2):c.1431del (p.Phe477fs)
|
rs1762258987
|
|
|
NM_001046.3(SLC12A2):c.2006-1G>A
|
rs1762648450
|
|
|
NM_001046.3(SLC12A2):c.2107+11A>G
|
rs189093520
|
|
|
NM_001046.3(SLC12A2):c.2361T>G (p.Phe787Leu)
|
|
|
|
NM_001046.3(SLC12A2):c.2617-2A>G
|
|
|
|
NM_001046.3(SLC12A2):c.2756T>C (p.Val919Ala)
|
|
|
|
NM_001046.3(SLC12A2):c.2848G>A (p.Val950Met)
|
rs760024899
|
|
|
NM_001046.3(SLC12A2):c.288GGC[10] (p.Ala105_Ala107dup)
|
rs746633185
|
|
|
NM_001046.3(SLC12A2):c.288GGC[11] (p.Ala104_Ala107dup)
|
rs746633185
|
|
|
NM_001046.3(SLC12A2):c.2894C>A (p.Ser965Tyr)
|
|
|
|
NM_001046.3(SLC12A2):c.2962C>A (p.Pro988Thr)
|
rs1581138965
|
|
|
NM_001046.3(SLC12A2):c.3134C>T (p.Thr1045Ile)
|
|
|
|
NM_001046.3(SLC12A2):c.3566C>T (p.Ala1189Val)
|
rs768256710
|
|
|
NM_001046.3(SLC12A2):c.3622C>G (p.Leu1208Val)
|
rs761150347
|
|
|
NM_001046.3(SLC12A2):c.476C>T (p.Ala159Val)
|
|
|
|
NM_001046.3(SLC12A2):c.562GGC[6] (p.Gly192dup)
|
rs751759733
|
|
|
NM_001046.3(SLC12A2):c.881G>A (p.Arg294His)
|
rs1484832467
|
|
|
NM_001046.3(SLC12A2):c.959C>A (p.Ser320Ter)
|
|
|
|
Single allele
|
|
|