ClinVar Miner

Variants from Reutter Lab, Institute of Human Genetics,University Hospital Bonn

Location: Germany — Primary collection method: research
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 total
4 5 3 15 0 27

Gene and significance breakdown #

Total genes and gene combinations: 27
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign total
AATF, ACACA, C17orf78, DDX52, DHRS11, DUSP14, GGNBP2, HNF1B, LHX1, MRM1, MYO19, PIGW, SYNRG, TADA2A, ZNHIT3 1 0 0 0 1
ABR, BHLHA9, TRARG1, YWHAE 0 0 0 1 1
ACTB 1 0 0 0 1
AGMO 0 0 0 1 1
AIFM3, ARVCF, C22orf39, CDC45, CLDN5, CLTCL1, COMT, CRKL, DGCR2, DGCR6L, DGCR8, ESS2, FAM230A, GGTLC3, GNB1L, GP1BB, GSC2, HIRA, KLHL22, LZTR1, MED15, MRPL40, P2RX6, PI4KA, PRODH, RANBP1, RIMBP3, RTL10, RTN4R, SCARF2, SEPTIN5, SERPIND1, SLC25A1, SLC7A4, SNAP29, TANGO2, TBX1, THAP7, TMEM191B, TRMT2A, TSSK2, TXNRD2, UFD1, USP41, ZDHHC8, ZNF74 0 1 0 0 1
ALPK3, NMB, PDE8A, SEC11A, SLC28A1, WDR73, ZNF592, ZSCAN2 0 0 0 1 1
ANKS1B, UHRF1BP1L 0 0 0 1 1
B3GNTL1, METRNL, TBCD 0 0 0 1 1
BAZ1A 1 0 0 0 1
CCDC74A, MZT2A, TUBA3D 0 0 0 1 1
CDH13 0 1 0 0 1
CNTNAP2 0 0 0 1 1
DLG3 0 0 1 0 1
DNAJC15, EPSTI1 0 0 0 1 1
FAM170A 0 1 0 0 1
FBP1, FBP2 0 0 0 1 1
FOXF1 0 1 0 0 1
FXYD4, HNRNPF 0 1 0 0 1
GPC5 0 0 0 1 1
NALCN 0 0 0 1 1
NBAS 0 0 1 0 1
NREP 0 0 0 1 1
PARM1 0 0 0 1 1
SCN9A 0 0 1 0 1
SMYD3 0 0 0 1 1
SORCS1 0 0 0 1 1
ZIC3 1 0 0 0 1

Condition and significance breakdown #

Total conditions: 8
Download table as spreadsheet
Condition pathogenic likely pathogenic uncertain significance likely benign total
VATER association 1 5 0 15 21
Baraitser-Winter syndrome 1 1 0 0 0 1
Infantile liver failure syndrome 2 0 0 1 0 1
Primary erythromelalgia 0 0 1 0 1
Short stature, optic nerve atrophy, and Pelger-Huet anomaly 0 0 1 0 1
VACTERL association with hydrocephaly, X-linked 1 0 0 0 1
VATER/VACTERL association with CNS malformations 1 0 0 0 1
X-Linked mental retardation 90 0 0 1 0 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.