List of variants in gene SLC25A4 reported as benign for ocular motility disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_001151.4(SLC25A4):c.*512A>G	rs7660552	0.90870
NM_001151.4(SLC25A4):c.*2307T>C	rs2046535	0.42438
NM_001151.4(SLC25A4):c.*2943G>A	rs7675110	0.42427
NM_001151.4(SLC25A4):c.*1053T>C	rs55905558	0.42184
NM_001151.4(SLC25A4):c.-25G>A	rs3733652	0.04735
NM_001151.4(SLC25A4):c.*873G>A	rs76680834	0.02960
NM_001151.4(SLC25A4):c.*3114C>A	rs147626367	0.02525
NM_001151.4(SLC25A4):c.*957T>C	rs11930741	0.01671
NM_001151.4(SLC25A4):c.*2050A>G	rs76364770	0.01609
NM_001151.4(SLC25A4):c.681G>A (p.Val227=)	rs34486484	0.00972
NM_001151.4(SLC25A4):c.567T>C (p.Ala189=)	rs149101873	0.00911
NM_001151.4(SLC25A4):c.*2476G>A	rs76335670	0.00573
NM_001151.4(SLC25A4):c.*2529C>T	rs113950388	0.00401
NM_001151.4(SLC25A4):c.*1792C>A	rs3733653	0.00213
NM_001151.4(SLC25A4):c.173_174del	rs112970805	0.00148
NM_001151.4(SLC25A4):c.*1985T>C	rs3733654	0.00133
NM_001151.4(SLC25A4):c.*2466C>A	rs142255349	0.00054
NM_001151.4(SLC25A4):c.*3110G>C	rs116996106	0.00042
NM_001151.4(SLC25A4):c.*1245T>A	rs77959660	0.00041
NM_001151.4(SLC25A4):c.756G>A (p.Thr252=)	rs150786764	0.00011
NM_001151.4(SLC25A4):c.*3070C>T	rs539027516	0.00004
NM_001151.4(SLC25A4):c.*1146T>C	rs537652975	0.00002
NM_001151.4(SLC25A4):c.*497T>G	rs562129249	0.00001
NM_001151.4(SLC25A4):c.*277C>T	rs190251889
NM_001151.4(SLC25A4):c.*323TTA[1]	rs139462979
NM_001151.4(SLC25A4):c.*481G>T	rs78882199

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