ClinVar Miner

List of variants in gene RAC2 reported as likely benign for immune system disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002872.5(RAC2):c.226-16C>T rs201500108 0.00046
NM_002872.5(RAC2):c.507C>T (p.Phe169=) rs150782757 0.00029
NM_002872.5(RAC2):c.545C>T (p.Thr182Met) rs141308774 0.00012
NM_002872.5(RAC2):c.147G>A (p.Lys49=) rs140543568 0.00010
NM_002872.5(RAC2):c.78C>T (p.Asn26=) rs375093215 0.00005
NM_002872.5(RAC2):c.282C>T (p.Arg94=) rs201989515 0.00004
NM_002872.5(RAC2):c.226-18C>T rs776743351 0.00003
NM_002872.5(RAC2):c.561C>T (p.Arg187=) rs201536161 0.00003
NM_002872.5(RAC2):c.192C>T (p.Tyr64=) rs772302068 0.00002
NM_002872.5(RAC2):c.276C>T (p.Asn92=) rs768931430 0.00002
NM_002872.5(RAC2):c.525C>T (p.Ala175=) rs575699146 0.00002
NM_002872.5(RAC2):c.108-5C>G rs1268302473 0.00001
NM_002872.5(RAC2):c.186G>A (p.Glu62=) rs778182086 0.00001
NM_002872.5(RAC2):c.243C>T (p.Cys81=) rs1380331398 0.00001
NM_002872.5(RAC2):c.289-18C>T rs1927057532 0.00001
NM_002872.5(RAC2):c.334C>T (p.Leu112=) rs1927054600 0.00001
NM_002872.5(RAC2):c.348G>A (p.Lys116=) rs777290534 0.00001
NM_002872.5(RAC2):c.363C>T (p.Asp121=) rs771516943 0.00001
NM_002872.5(RAC2):c.364G>A (p.Asp122Asn) rs910521882 0.00001
NM_002872.5(RAC2):c.449-9C>T rs1420203399 0.00001
NM_002872.5(RAC2):c.510C>T (p.Asp170=) rs752897291 0.00001
NM_002872.5(RAC2):c.562G>A (p.Ala188Thr) rs758461304 0.00001
NM_002872.5(RAC2):c.579G>A (p.Ter193=) rs371789770 0.00001
NM_002872.5(RAC2):c.108-11G>A
NM_002872.5(RAC2):c.108-19C>T
NM_002872.5(RAC2):c.108-20G>A
NM_002872.5(RAC2):c.141C>T (p.Asp47=)
NM_002872.5(RAC2):c.162G>A (p.Gly54=)
NM_002872.5(RAC2):c.183G>A (p.Gln61=)
NM_002872.5(RAC2):c.207G>A (p.Pro69=) rs755454147
NM_002872.5(RAC2):c.207G>C (p.Pro69=)
NM_002872.5(RAC2):c.225+13C>T
NM_002872.5(RAC2):c.225+16C>T
NM_002872.5(RAC2):c.226-10C>G
NM_002872.5(RAC2):c.226-13G>T
NM_002872.5(RAC2):c.226-14T>C
NM_002872.5(RAC2):c.226-17G>A
NM_002872.5(RAC2):c.226-19_226-17del
NM_002872.5(RAC2):c.228C>T (p.Asp76=)
NM_002872.5(RAC2):c.249C>T (p.Ser83=)
NM_002872.5(RAC2):c.258C>T (p.Ser86=)
NM_002872.5(RAC2):c.261A>T (p.Pro87=)
NM_002872.5(RAC2):c.264C>G (p.Ala88=)
NM_002872.5(RAC2):c.288+10A>G rs2145824091
NM_002872.5(RAC2):c.288+11C>T
NM_002872.5(RAC2):c.288+11del
NM_002872.5(RAC2):c.288+14G>T
NM_002872.5(RAC2):c.288+15G>C rs1271458258
NM_002872.5(RAC2):c.288+16T>C
NM_002872.5(RAC2):c.289-6G>T
NM_002872.5(RAC2):c.333C>A (p.Ile111=)
NM_002872.5(RAC2):c.35+15G>T rs748808662
NM_002872.5(RAC2):c.35+20T>C
NM_002872.5(RAC2):c.35+20T>G rs747917580
NM_002872.5(RAC2):c.36-16A>G
NM_002872.5(RAC2):c.36-18G>A
NM_002872.5(RAC2):c.369G>A (p.Lys123=)
NM_002872.5(RAC2):c.378C>T (p.Ile126=)
NM_002872.5(RAC2):c.449-15C>T
NM_002872.5(RAC2):c.450C>T (p.Asp150=) rs781040687
NM_002872.5(RAC2):c.45C>T (p.Gly15=)
NM_002872.5(RAC2):c.474A>G (p.Ser158=) rs1195995740
NM_002872.5(RAC2):c.483C>T (p.Thr161=) rs1601667909
NM_002872.5(RAC2):c.501C>G (p.Thr167=)
NM_002872.5(RAC2):c.520C>A (p.Arg174=)
NM_002872.5(RAC2):c.522G>A (p.Arg174=)
NM_002872.5(RAC2):c.525C>G (p.Ala175=)
NM_002872.5(RAC2):c.528G>A (p.Val176=) rs2145819292
NM_002872.5(RAC2):c.546G>A (p.Thr182=)
NM_002872.5(RAC2):c.547C>A (p.Arg183=)
NM_002872.5(RAC2):c.54C>T (p.Cys18=)
NM_002872.5(RAC2):c.567C>T (p.Cys189=)
NM_002872.5(RAC2):c.75C>T (p.Thr25=)
NM_002872.5(RAC2):c.81C>A (p.Ala27=) rs2239774
NM_002872.5(RAC2):c.87C>T (p.Pro29=)

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.