ClinVar Miner

List of variants in gene HTRA2 studied for Parkinson disease

Included ClinVar conditions (34):
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Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_013247.4(HTRA2):c.-136C>G rs886056343
NM_013247.4(HTRA2):c.-146G>A rs569404179
NM_013247.4(HTRA2):c.-216G>A rs886056342
NM_013247.4(HTRA2):c.-236G>C rs886056341
NM_013247.4(HTRA2):c.-86G>C rs886056344
NM_013247.4(HTRA2):c.1046-13C>T rs542851656
NM_013247.4(HTRA2):c.215T>C (p.Leu72Pro) rs150047108
NM_013247.4(HTRA2):c.241G>A (p.Ala81Thr) rs886056345
NM_013247.4(HTRA2):c.354G>A (p.Leu118=) rs199735424
NM_013247.4(HTRA2):c.421G>T (p.Ala141Ser) rs72470544
NM_013247.4(HTRA2):c.427C>G (p.Pro143Ala) rs387906942
NM_013247.4(HTRA2):c.480C>G (p.Ala160=) rs2231248
NM_013247.4(HTRA2):c.507-10T>A rs747756166
NM_013247.4(HTRA2):c.507-9C>A rs151291127
NM_013247.4(HTRA2):c.510C>T (p.His170=) rs200747610
NM_013247.4(HTRA2):c.627A>G (p.Arg209=) rs149169879
NM_013247.4(HTRA2):c.825T>C (p.Val275=) rs777650346
NM_013247.4(HTRA2):c.873T>C (p.Asn291=) rs775948550
NM_013247.5(HTRA2):c.1046-5C>G
NM_013247.5(HTRA2):c.1056C>T (p.Ser352=)
NM_013247.5(HTRA2):c.1079G>A (p.Arg360His)
NM_013247.5(HTRA2):c.77G>A (p.Gly26Glu)
NM_013247.5(HTRA2):c.937C>T (p.Leu313=)
NM_145074.2(HTRA2):c.-136C>T

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