ClinVar Miner

List of variants reported as pathogenic for Pick disease by OMIM

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_000021.4(PSEN1):c.548G>T (p.Gly183Val) rs63751068
NM_016835.4(MAPT):c.1721A>C (p.Lys574Thr) rs63750129
NM_016835.4(MAPT):c.1910C>T (p.Ser637Phe) rs63750635
NM_016835.4(MAPT):c.2057A>T (p.Lys686Ile) rs63751264
NM_016835.4(MAPT):c.2116G>A (p.Gly706Arg) rs63750512

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