List of variants reported as benign for amyotrophic lateral sclerosis type 6 by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 35

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HGVS	dbSNP	gnomAD frequency
NM_004960.3(FUS):c.*1476T>C	rs11860134	0.98998
NM_004960.4(FUS):c.-54A>G	rs929867	0.95117
NM_004960.4(FUS):c.291C>T (p.Tyr97=)	rs1052352	0.45484
NM_004960.3(FUS):c.*770G>C	rs4889537	0.24493
NM_004960.4(FUS):c.147C>A (p.Gly49=)	rs741810	0.24179
NM_004960.4(FUS):c.190+9T>C	rs73530283	0.06048
NM_004960.3(FUS):c.*1803C>T	rs16956408	0.06040
NM_004960.4(FUS):c.153C>T (p.Gly51=)	rs61733962	0.03329
NM_004960.3(FUS):c.*491T>G	rs73530293	0.03268
NM_004960.3(FUS):c.*2486G>A	rs73530298	0.03248
NM_004960.3(FUS):c.*2794G>C	rs17839571	0.03244
NM_004960.3(FUS):c.*910C>T	rs118018900	0.02606
NM_004960.3(FUS):c.*2393T>A	rs541197027	0.01834
NM_004960.3(FUS):c.*989C>T	rs114772555	0.01702
NM_004960.3(FUS):c.*1420C>T	rs73530295	0.01500
NM_004960.4(FUS):c.1156C>A (p.Arg386=)	rs61733965	0.01496
NM_004960.4(FUS):c.524-5C>T	rs73530287	0.01495
NM_004960.4(FUS):c.-39A>G	rs67676356	0.01242
NM_004960.3(FUS):c.*626G>A	rs115626460	0.00863
NM_004960.3(FUS):c.*1148A>T	rs140326191	0.00506
NM_004960.3(FUS):c.*2443A>G	rs189787862	0.00503
NM_004960.3(FUS):c.*214C>T	rs140875749	0.00361
NM_004960.3(FUS):c.*2988C>T	rs73530301	0.00254
NM_004960.3(FUS):c.*687G>A	rs549602004	0.00193
NM_004960.4(FUS):c.675C>T (p.Gly225=)	rs140003720	0.00179
NM_004960.4(FUS):c.1566G>A (p.Arg522=)	rs138901914	0.00095
NM_004960.4(FUS):c.-47G>A	rs72550864	0.00081
NM_004960.4(FUS):c.1464C>T (p.Gly488=)	rs150529460	0.00075
NM_004960.4(FUS):c.198T>C (p.Tyr66=)	rs144853447	0.00056
NM_004960.3(FUS):c.*3231T>C	rs193018950	0.00041
NM_004960.4(FUS):c.764+12A>C	rs143916861	0.00024
NM_004960.3(FUS):c.*1883T>C	rs549012470	0.00004
NM_004960.3(FUS):c.*2884A>T	rs554281103	0.00004
NM_004960.4(FUS):c.*10C>T	rs529269129	0.00002
NM_004960.3(FUS):c.*3230A>G	rs550798081

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