ClinVar Miner

List of variants reported as not provided for Preeclampsia

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ClinVar version:
Total variants: 83
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HGVS dbSNP gnomAD frequency
CM000663.1:g.3411413_3431235dup
CM000664.1:g.223798501_223823141dup
CM000665.1:g.100351696_100437892dup
CM000673.1:g.42151229_42185849dup
GRCh37/hg19 12q24.31(chr12:125260645-125321461)x3
NC_000001.11:g.111383531_111391682del
NC_000001.11:g.40877936_40912404dup
NC_000002.11:g.89427986_90240473dup
NC_000002.11:g.89427986_91820358dup
NC_000002.12:g.49630800_49638002del
NC_000003.12:g.149246905_149249548del
NC_000003.12:g.35785215_35861393dup
NC_000004.12:g.45815310_45861251dup
NC_000006.12:g.14839547_14845568del
NC_000006.12:g.19045329_19048542del
NC_000007.14:g.146096986_146099665del
NC_000007.14:g.19166813_19172086del
NC_000007.14:g.62533792_63268846dup
NC_000008.11:g.16042179_16081673dup
NC_000008.11:g.16405000_16410993del
NC_000008.11:g.5741877_5750141del
NC_000008.11:g.5741877_5750560del
NC_000008.11:g.8725600_8730080del
NC_000009.12:g.83588331_83591428del
NC_000010.11:g.133438843_133565298dup
NC_000011.10:g.83154476_83165228dup
NC_000011.10:g.8937474_8943392del
NC_000011.10:g.97981770_98652344del
NC_000012.12:g.128744329_128749559del
NC_000012.12:g.31106438_31256645dup
NC_000012.12:g.31113353_31255762dup
NC_000012.12:g.63548869_63724778dup
NC_000012.12:g.7777575_7949790dup
NC_000013.11:g.58019523_58024897del
NC_000013.11:g.83214607_83217480del
NC_000013.11:g.85294188_85330291dup
NC_000014.9:g.40385828_40389224del
NC_000014.9:g.90322590_90335706dup
NC_000015.10:g.24349669_24497505dup
NC_000015.10:g.81685124_81795773dup
NC_000015.9:g.23084443_23114374del
NC_000016.10:g.28592568_28609431dup
NC_000017.11:g.46092442_46502770dup
NC_000017.11:g.52872255_53236993del
NC_000017.11:g.79371616_79397955dup
NC_000018.10:g.30235355_30236003del rs1555628672
NC_000018.10:g.66182443_66199550dup
NC_000018.10:g.69080332_69088272del
NC_000021.8:g.35027142_35056247del
NM_000719.7(CACNA1C):c.477+16040_477+23328del
NM_000762.5(CYP2A6):c.-22817_-420del
NM_001004708.1(OR4D6):c.-19514_20175del
NM_001008392.2(CTDSPL):c.80-8666_80-2299del
NM_001010848.3(NRG3):c.824-173790_824-159316del
NM_001025616.2(ARHGAP24):c.-186452_-21+35669dup
NM_001135924.3(VWDE):c.541+441_879+501del
NM_001145728.2(LMNTD1):c.*22+2227_*22+7996del
NM_001164405.1(BHLHA9):c.-56867_66089del
NM_001244606.1(IMMP2L):c.239+53584_239+101346del
NM_001267803.1(PAAF1):c.*451_*70114dup
NM_001282805.1(MARCH7):c.-247472_-1723dup
NM_001363059.2(MTUS1):c.2288-795_2449+390del
NM_002531.2(NTSR1):c.*2254_*20847del
NM_005100.4(AKAP12):c.163-8647_163-5271del
NM_014932.4(NLGN1):c.-320-82616_-320-21032dup
NM_015194.3(MYO1D):c.2865-44956_2865-37036del
NM_016316.4(REV1):c.351-3232_513dup
NM_016329.4(SFMBT1):c.-130-31769_-130-30020del
NM_018012.4(KIF26B):c.1166+53868_1166+59172del
NM_018557.3(LRP1B):c.344-65793_344-61550del
NM_021156.3(TMX4):c.*826_*5132dup
NM_024795.3(TM4SF20):c.-14304_183+492dup
NM_139265.3(EHD4):c.*803_*33733dup
NM_144682.5(SLFN13):c.2109_*83579del
NM_152721.6(DOK6):c.67-22582_67-14452del
NM_178466.5(BPIFA3):c.127+1119_621+52del
NR_002812.3(HCG26):n.-83887_14635dup
NR_031714.1(MIR1324):n.-251239_47012del
NR_037466.1(MIR3180-4):n.-250198_93962del
NR_110592.1(LINC01238):n.972-495_131503del
NR_125764.1(LINC01322):n.201-50931_201-19041del
NR_135237.1(LOC730100):n.754-62628_754-62323del rs1553354646
Single allele

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