ClinVar Miner

List of variants reported as uncertain significance for FADD-related immunodeficiency by Invitae

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP
NM_003824.3(FADD):c.168G>T (p.Glu56Asp) rs777501231
NM_003824.3(FADD):c.306C>G (p.Asn102Lys) rs775250989
NM_003824.3(FADD):c.307G>A (p.Val103Ile) rs200845739
NM_003824.3(FADD):c.31G>A (p.Val11Met) rs753665798
NM_003824.3(FADD):c.439A>G (p.Ile147Val) rs140822085
NM_003824.3(FADD):c.452C>T (p.Thr151Ile) rs150178083
NM_003824.3(FADD):c.475G>A (p.Ala159Thr) rs1555063819
NM_003824.4(FADD):c.248A>G (p.Glu83Gly)
NM_003824.4(FADD):c.324G>A (p.Val108=)
NM_003824.4(FADD):c.378C>G (p.Ile126Met)
NM_003824.4(FADD):c.51C>G (p.Ser17Arg)
NM_003824.4(FADD):c.52A>C (p.Ser18Arg)

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.