List of variants reported as likely benign for Lewy body dementia

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_000157.4(GBA1):c.762-18T>A	rs140335079	0.00896
NM_000345.4(SNCA):c.*139T>G	rs10024743	0.00703
NM_000157.4(GBA1):c.1444G>A (p.Asp482Asn)	rs75671029	0.00236
NM_000157.4(GBA1):c.1473C>T (p.Pro491=)	rs149257166	0.00094
NM_000345.4(SNCA):c.121+11C>T	rs35135226	0.00022
NM_000345.4(SNCA):c.216G>A (p.Thr72=)	rs144758871	0.00021
NM_000345.4(SNCA):c.156G>T (p.Val52=)	rs148108612	0.00019
NM_000345.4(SNCA):c.147G>A (p.Val49=)	rs141859659	0.00015
NM_000345.4(SNCA):c.298T>C (p.Leu100=)	rs138969470	0.00014
NM_000345.4(SNCA):c.391-16A>G	rs371014092	0.00006
NM_000345.4(SNCA):c.121+13C>T	rs763539470	0.00003
NM_000345.4(SNCA):c.225A>T (p.Thr75=)	rs149401968	0.00003
NM_000345.4(SNCA):c.390+11A>C	rs546366532	0.00002
NM_000345.4(SNCA):c.246G>A (p.Val82=)	rs775179895	0.00001
NM_000345.4(SNCA):c.306+8T>C	rs758513669	0.00001
NM_000157.4(GBA1):c.*92G>A
NM_000345.4(SNCA):c.*77C>A	rs145304567
NM_000345.4(SNCA):c.105G>A (p.Glu35=)
NM_000345.4(SNCA):c.121+9A>C
NM_000345.4(SNCA):c.163+7T>G	rs1578405610
NM_000345.4(SNCA):c.164-16T>A
NM_000345.4(SNCA):c.243A>G (p.Thr81=)	rs568436589
NM_000345.4(SNCA):c.306+20G>A
NM_000345.4(SNCA):c.306+7C>T	rs2110460139
NM_000345.4(SNCA):c.307-13C>T
NM_000345.4(SNCA):c.349C>T (p.Pro117Ser)
NM_000345.4(SNCA):c.375T>C (p.Tyr125=)
NM_000345.4(SNCA):c.381G>A (p.Met127Ile)
NM_000345.4(SNCA):c.390+7G>C
NM_000345.4(SNCA):c.396G>T (p.Gly132=)
NM_000345.4(SNCA):c.99A>G (p.Thr33=)
NM_000345.4(SNCA):c.9A>G (p.Val3=)

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