NM_002303.6(LEPR):c.371A>G (p.Asp124Gly)
|
rs35573508
|
0.00192
|
NM_000439.5(PCSK1):c.1918A>G (p.Thr640Ala)
|
rs139453594
|
0.00157
|
NM_000439.5(PCSK1):c.1387G>A (p.Glu463Lys)
|
rs143174906
|
0.00085
|
NM_017780.4(CHD7):c.7595C>T (p.Thr2532Met)
|
rs201032343
|
0.00062
|
NM_002303.6(LEPR):c.2918C>A (p.Thr973Asn)
|
rs142143966
|
0.00055
|
NM_173648.4(CCDC141):c.538C>T (p.Arg180Trp)
|
rs768401425
|
0.00012
|
NM_001166114.2(PNPLA6):c.1430C>T (p.Ser477Leu)
|
rs140929996
|
0.00004
|
NM_001166114.2(PNPLA6):c.29C>G (p.Thr10Arg)
|
rs777466386
|
0.00004
|
NM_017780.4(CHD7):c.1696C>G (p.Pro566Ala)
|
rs764518030
|
0.00001
|
NM_019066.5(MAGEL2):c.220G>A (p.Ala74Thr)
|
rs1216919340
|
0.00001
|
NM_019066.5(MAGEL2):c.2343G>T (p.Glu781Asp)
|
rs772413215
|
0.00001
|
NM_019066.5(MAGEL2):c.2363G>T (p.Ser788Ile)
|
rs984557516
|
0.00001
|
NM_000439.5(PCSK1):c.1381G>A (p.Val461Met)
|
|
|
NM_000439.5(PCSK1):c.1430+7A>G
|
|
|
NM_000439.5(PCSK1):c.638C>T (p.Ala213Val)
|
|
|
NM_002303.6(LEPR):c.1012C>A (p.Pro338Thr)
|
|
|
NM_002303.6(LEPR):c.3240A>C (p.Leu1080Phe)
|
|
|
NM_002303.6(LEPR):c.346A>C (p.Asn116His)
|
|
|
NM_002303.6(LEPR):c.495-2927T>G
|
|
|
NM_002303.6(LEPR):c.976C>T (p.Arg326Cys)
|
|
|
NM_017780.4(CHD7):c.1577A>G (p.Gln526Arg)
|
rs2150581368
|
|
NM_017780.4(CHD7):c.4771C>T (p.Pro1591Ser)
|
rs2150786767
|
|
NM_017780.4(CHD7):c.6598G>C (p.Gly2200Arg)
|
rs747357928
|
|
NM_017780.4(CHD7):c.7465C>A (p.Leu2489Ile)
|
|
|
NM_017780.4(CHD7):c.7503C>G (p.Ser2501=)
|
rs1805737676
|
|
NM_019066.5(MAGEL2):c.1445C>T (p.Ala482Val)
|
rs2140716042
|
|
NM_019066.5(MAGEL2):c.1991C>T (p.Pro664Leu)
|
rs201935129
|
|
NM_019066.5(MAGEL2):c.2587C>A (p.Gln863Lys)
|
|
|
NM_019066.5(MAGEL2):c.2746A>G (p.Asn916Asp)
|
rs2140713261
|
|
NM_019066.5(MAGEL2):c.293_294delinsAT (p.Pro98His)
|
|
|
NM_019066.5(MAGEL2):c.3384G>C (p.Arg1128Ser)
|
rs1357977229
|
|
NM_019066.5(MAGEL2):c.3661G>A (p.Ala1221Thr)
|
rs779840896
|
|
NM_019066.5(MAGEL2):c.509_510delinsTG (p.Ala170Val)
|
rs2140718561
|
|
NM_019066.5(MAGEL2):c.623C>A (p.Pro208Gln)
|
|
|
NM_019066.5(MAGEL2):c.992C>T (p.Pro331Leu)
|
|
|
NM_033343.4(LHX4):c.464C>T (p.Ala155Val)
|
rs746041842
|
|
NM_173648.4(CCDC141):c.4312C>T (p.Pro1438Ser)
|
rs1684498900
|
|