ClinVar Miner

List of variants in gene combination GH-LCR, SCN4A reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
NM_000334.4(SCN4A):c.2350A>G (p.Met784Val) rs1567822938
NM_000334.4(SCN4A):c.2697G>A (p.Leu899=) rs199827271
NM_000334.4(SCN4A):c.2846A>G (p.Asp949Gly) rs1555602253
NM_000334.4(SCN4A):c.3038G>A (p.Arg1013His) rs578232775
NM_000334.4(SCN4A):c.4106C>A (p.Thr1369Asn) rs748313755
NM_000334.4(SCN4A):c.5000C>T (p.Pro1667Leu) rs765721076
NM_000334.4(SCN4A):c.5468C>G (p.Pro1823Arg) rs376833596

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.