ClinVar Miner

Variants from Australian Red Cross Blood Service

Location: Australia  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 affects association risk factor total
1 0 3 0 0 22 1 1 28

Gene and significance breakdown #

Total genes and gene combinations: 14
Download table as spreadsheet
Gene or gene combination pathogenic uncertain significance affects association risk factor total
RHD, RSRP1 0 0 6 0 1 7
KEL 0 1 5 0 0 6
ABCB6 0 0 2 0 0 2
ABO 0 0 2 0 0 2
SLC14A1 0 1 1 0 0 2
ACKR1 0 0 1 0 0 1
CD55 0 0 1 0 0 1
GYPB 0 0 0 1 0 1
ICAM4 0 1 0 0 0 1
KLF1, LOC117125591 0 0 1 0 0 1
KLF1, LOC130063673 0 0 1 0 0 1
POLR1C, SLC29A1 1 0 0 0 0 1
RHAG 0 0 1 0 0 1
RHCE 0 0 1 0 0 1

Condition and significance breakdown #

Total conditions: 19
Download table as spreadsheet
Condition pathogenic uncertain significance affects association risk factor total
Kell blood group system 0 1 4 0 0 5
weakened D expression by serology 0 0 3 0 0 3
ABO blood group system 0 0 2 0 0 2
BLOOD GROUP--LUTHERAN INHIBITOR 0 0 2 0 0 2
Langereis blood group 0 0 2 0 0 2
altered red cell phenotype 0 0 2 0 0 2
Anti-D isoimmunization affecting pregnancy 0 0 0 0 1 1
BLOOD GROUP, Ss 0 0 0 1 0 1
BLOOD GROUP--KIDD SYSTEM 0 1 0 0 0 1
Blood group antigen abnormality 0 0 1 0 0 1
Cromer blood group system 0 0 1 0 0 1
Duffy Blood group system 0 0 1 0 0 1
Hemolytic disease of fetus OR newborn due to RhD isoimmunization 0 0 0 0 1 1
Hemolytic disease of fetus OR newborn due to isoimmunization 1 0 0 0 0 1
Landsteiner-Wiener phenotype 0 1 0 0 0 1
Weakened expression of D antigen 0 0 1 0 0 1
altered RHD phenotype 0 0 1 0 0 1
altered RhC expression 0 0 1 0 0 1
not provided 0 0 1 0 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.