ClinVar Miner

List of variants in gene SNCA reported as likely benign for Lewy body dementia

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_000345.4(SNCA):c.*139T>G rs10024743 0.00703
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_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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