ClinVar Miner

List of variants reported as benign for hereditary spastic paraplegia 6 by Illumina Laboratory Services, Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_144599.5(NIPA1):c.*1981A>G rs6606822 0.99970
NM_144599.5(NIPA1):c.*1974C>A rs6606823 0.93707
NM_144599.5(NIPA1):c.441A>G (p.Thr147=) rs11263683 0.65973
NM_144599.5(NIPA1):c.*972C>T rs8025849 0.64186
NM_144599.5(NIPA1):c.*4933C>T rs7181789 0.57163
NM_144599.5(NIPA1):c.*1127C>G rs1059774 0.32452
NM_144599.5(NIPA1):c.*1927A>G rs17807140 0.28781
NM_144599.5(NIPA1):c.*287T>C rs3812924 0.22372
NM_144599.5(NIPA1):c.*2425A>G rs12902722 0.10277
NM_144599.5(NIPA1):c.*1563C>T rs72698098 0.09246
NM_144599.5(NIPA1):c.*3702C>T rs3812923 0.03905
NM_144599.5(NIPA1):c.*3278C>G rs57615013 0.02793
NM_144599.5(NIPA1):c.*2649A>G rs8027756 0.02539
NM_144599.5(NIPA1):c.*5331T>G rs73412681 0.02493
NM_144599.5(NIPA1):c.*5299G>C rs73412682 0.02437
NM_144599.5(NIPA1):c.*4734G>C rs73412685 0.02429
NM_144599.5(NIPA1):c.*2469A>G rs73412688 0.02406
NM_144599.5(NIPA1):c.*1405G>C rs7181585 0.01455
NM_144599.5(NIPA1):c.*4363C>T rs139459875 0.00774
NM_144599.5(NIPA1):c.*3910G>A rs74767096 0.00528
NM_144599.5(NIPA1):c.*3393A>T rs147611065 0.00409
NM_144599.5(NIPA1):c.*1012A>G rs186626641 0.00401
NM_144599.5(NIPA1):c.*5237G>C rs74003089 0.00338
NM_144599.5(NIPA1):c.*5044G>C rs191543264 0.00270
NM_144599.5(NIPA1):c.*4218G>A rs182099304 0.00260
NM_144599.5(NIPA1):c.*3480C>T rs112696483 0.00216
NM_144599.5(NIPA1):c.*2780G>T rs183353690 0.00189
NM_144599.5(NIPA1):c.*5071C>T rs141920126 0.00185
NM_144599.5(NIPA1):c.*4964G>A rs146129067 0.00179
NM_144599.5(NIPA1):c.*3590A>G rs145202306 0.00130
NM_144599.5(NIPA1):c.*4885T>C rs555159081 0.00111
NM_144599.5(NIPA1):c.906C>T (p.Ser302=) rs147070285 0.00087
NM_144599.5(NIPA1):c.*1724C>G rs61523596 0.00069
NM_144599.5(NIPA1):c.*4774G>A rs541776619 0.00067
NM_144599.5(NIPA1):c.*4716G>A rs540912938 0.00055
NM_144599.5(NIPA1):c.*3400C>T rs577663387 0.00029
NM_144599.5(NIPA1):c.*11G>C rs188393827 0.00026
NM_144599.5(NIPA1):c.*1395C>T rs537516417 0.00021
NM_144599.5(NIPA1):c.801G>T (p.Val267=) rs185222838 0.00020
NM_144599.5(NIPA1):c.*3872T>G rs528309949 0.00013
NM_144599.5(NIPA1):c.*4792G>T rs139161065 0.00008
NM_144599.5(NIPA1):c.*1146T>C rs181621508 0.00006
NM_144599.5(NIPA1):c.*2515G>C rs6606820
NM_144599.5(NIPA1):c.*4510T>C rs528249723

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