ClinVar Miner

List of variants in gene CRB2 studied for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
NM_173689.7(CRB2):c.1151G>T (p.Cys384Phe)
NM_173689.7(CRB2):c.1600C>T (p.Arg534Trp) rs759002273
NM_173689.7(CRB2):c.1859G>C (p.Cys620Ser) rs879255250
NM_173689.7(CRB2):c.1882C>T (p.Arg628Cys) rs202128397
NM_173689.7(CRB2):c.1886G>C (p.Cys629Ser) rs879255252
NM_173689.7(CRB2):c.1897C>T (p.Arg633Trp) rs730880377
NM_173689.7(CRB2):c.1928A>C (p.Glu643Ala) rs730880300
NM_173689.7(CRB2):c.2277G>A (p.Trp759Ter) rs375072557
NM_173689.7(CRB2):c.2400C>G (p.Asn800Lys) rs765676223
NM_173689.7(CRB2):c.3089_3104dup (p.Gly1036fs) rs879255251
NM_173689.7(CRB2):c.3190C>T (p.Pro1064Ser) rs868484209
NM_173689.7(CRB2):c.3559A>C (p.Thr1187Pro) rs1554785663
NM_173689.7(CRB2):c.3613G>A (p.Gly1205Ser)
NM_173689.7(CRB2):c.3746G>A (p.Arg1249Gln) rs147412276
NM_173689.7(CRB2):c.47_53dup (p.Leu19fs)

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.