ClinVar Miner

List of variants reported as uncertain significance for Pick disease

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_000021.3(PSEN1):c.104G>A (p.Arg35Gln) rs63750592
NM_000021.3(PSEN1):c.1148T>G (p.Leu383Trp)
NM_000021.3(PSEN1):c.532T>C (p.Ser178Pro) rs63750155
NM_001123066.3(MAPT):c.623delG (p.Gly208Alafs) rs773149360
NM_005910.5(MAPT):c.374-3346C>T rs377402921
NM_016841.4(MAPT):c.47G>T (p.Gly16Val) rs755131800

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