ClinVar Miner

Variants in gene combination LOC101927870, RELN with conflicting interpretations reported as "uncertain significance and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 10
Download table as spreadsheet
HGVS dbSNP
NM_005045.4(RELN):c.10026G>A (p.Thr3342=) rs542352292
NM_005045.4(RELN):c.10093G>A (p.Val3365Ile) rs115035120
NM_005045.4(RELN):c.8154A>T (p.Thr2718=) rs1554367205
NM_005045.4(RELN):c.8667+9_8667+13del rs755797350
NM_005045.4(RELN):c.8863C>T (p.Arg2955Cys) rs114501042
NM_005045.4(RELN):c.9172T>C (p.Leu3058=) rs2286261
NM_005045.4(RELN):c.9340A>G (p.Ile3114Val) rs149613347
NM_005045.4(RELN):c.9414C>T (p.Ser3138=) rs375427974
NM_005045.4(RELN):c.9524A>C (p.His3175Pro) rs74513461
NM_005045.4(RELN):c.9825C>T (p.Ser3275=) rs149713137

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.