ClinVar Miner

Variants studied for HELLP syndrome

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign not provided total
0 1 0 0 0 139 140

Gene and significance breakdown #

Total genes and gene combinations: 74
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Gene or gene combination likely pathogenic not provided total
​intergenic 0 66 66
ZDHHC11 0 2 2
ABR, BHLHA9, TRARG1 0 1 1
ACSL3 0 1 1
ADGRG7, TFG 0 1 1
AGAP10, ANXA8L1, NPY4R 0 1 1
AKAP12 0 1 1
ARHGAP11B, CHRFAM7A, GOLGA8H, GOLGA8J, GOLGA8Q, GOLGA8R, GOLGA8T, LINC02249, LOC100996413, LOC102725021, LOC106736464, LOC106736465, LOC106736468, LOC106736476, LOC106736480, LOC106783506 0 1 1
ARHGAP24 0 1 1
ARL17A, ARL17B, KANSL1, LOC112533643, LRRC37A 0 1 1
ARPP21 0 1 1
ASCL3 0 1 1
ATP8B3 0 1 1
BAZ2B, LOC643072 0 1 1
BPIFA3 0 1 1
C17orf112, LINC02089 0 1 1
CACNA1C 0 1 1
CATSPER2, STRC 0 1 1
CCDC102B 0 1 1
CD160, PDZK1, RNF115 0 1 1
CTDSPL 0 1 1
CYP2E1, LOC110599585, SYCE1 0 1 1
DNAJB13, PAAF1, UCP2 0 1 1
DOK6 0 1 1
DPY19L2, LOC108720144 0 1 1
EHD4, LOC105370792, SPTBN5 0 1 1
FRG2C, LINC00960, LINC02018, LOC112935961, MIR1324 0 1 1
GRIN2A 0 1 1
HCG26, HCP5, LINC01149, MICA, MICB-DT 0 1 1
IMMP2L 0 1 1
ITSN1 0 1 1
KIF26B 0 1 1
LINC00659, NTSR1 0 1 1
LINC01237, LINC01238, LINC01880, LINC01881, LOC285097 0 1 1
LINC01322 0 1 1
LINC01957, LOC101927078 0 1 1
LINC02018, LOC112935961 0 1 1
LINC02112 0 1 1
LMNTD1 0 1 1
LOC100505915, LOC112340378, MIR3180-4, MIR6511B2, MPV17L, NPIPA5, PDXDC1, RRN3 0 1 1
LOC108281140, MEGF6 0 1 1
LOC108942766, NANOG, SLC2A14, SLC2A3 0 1 1
LOC110673974 0 1 1
LOC111828495, SAFB2, TINCR 0 1 1
LOC112340392, SULT1A1, SULT1A2 0 1 1
LOC730100 0 1 1
LRP1B 0 1 1
MGAM 0 1 1
MTUS1 0 1 1
MYO1D 0 1 1
NHSL1 0 1 1
NIPA1 0 1 1
NLGN1 0 1 1
NRDE2 0 1 1
NRG3 0 1 1
NSD1 1 0 1
OR4C12 0 1 1
OR4D6, OR5A1 0 1 1
PCF11 0 1 1
PSG1, PSG11, PSG6, PSG7 0 1 1
PSG1, PSG6, PSG7 0 1 1
PSG4, PSG5 0 1 1
PWRN3 0 1 1
RBFOX3 0 1 1
REV1 0 1 1
SCARB1 0 1 1
SFMBT1 0 1 1
SLFN11, SLFN12, SLFN13 0 1 1
SOX11 0 1 1
TM4SF20 0 1 1
TMX4 0 1 1
TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D 0 1 1
VWDE 0 1 1
ZNF716 0 1 1

Submitter and significance breakdown #

Total submitters: 2
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Submitter likely pathogenic not provided total
Institute of Molecular and Cell Biology, University of Tartu 0 139 139
Centre for Mendelian Genomics,University Medical Centre Ljubljana 1 0 1

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