ClinVar Miner

List of variants in gene DNAJC6 reported as benign for Parkinson disease

Included ClinVar conditions (41):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_001256864.2(DNAJC6):c.2010A>C (p.Pro670=) rs4582839 0.69474
NM_001256864.2(DNAJC6):c.194-21G>T rs2296478 0.58031
NM_001256864.2(DNAJC6):c.194-19T>G rs2296479 0.57220
NM_001256864.2(DNAJC6):c.1500G>A (p.Glu500=) rs4325172 0.44325
NM_001256864.2(DNAJC6):c.544-9C>T rs2296481 0.25003
NM_001256864.2(DNAJC6):c.2183G>A (p.Ser728Asn) rs4915691 0.20494
NM_001256864.2(DNAJC6):c.1983T>C (p.Ser661=) rs12077111 0.17885
NM_001256864.2(DNAJC6):c.1506C>T (p.His502=) rs11208644 0.17883
NM_001256864.2(DNAJC6):c.194-20_194-19insG rs111346712 0.03019
NM_001256864.2(DNAJC6):c.678G>A (p.Ala226=) rs61753391 0.01829
NM_001256864.2(DNAJC6):c.1710G>A (p.Pro570=) rs7551930 0.01341
NM_001256864.2(DNAJC6):c.1456C>T (p.Leu486Phe) rs78141380 0.01170
NM_001256864.2(DNAJC6):c.1320A>T (p.Thr440=) rs142136708 0.00462
NM_001256864.2(DNAJC6):c.745A>G (p.Ile249Val) rs149588872 0.00357
NM_001256864.2(DNAJC6):c.194-18T>G rs201249130 0.00252
NM_001256864.2(DNAJC6):c.996-9T>C rs187965193 0.00178
NM_001256864.2(DNAJC6):c.513G>A (p.Lys171=) rs148204207 0.00101
NM_001256864.2(DNAJC6):c.1266A>T (p.Leu422=) rs61758427 0.00078
NM_001256864.2(DNAJC6):c.2451T>G (p.Pro817=) rs61733018 0.00076
NM_001256864.2(DNAJC6):c.194-17T>G rs372128441 0.00032
NM_001256864.2(DNAJC6):c.2331C>T (p.Gly777=) rs370155769 0.00003
NM_001256864.2(DNAJC6):c.1041C>A (p.Ile347=)
NM_001256864.2(DNAJC6):c.194-6del rs58549467
NM_001256864.2(DNAJC6):c.194-7_194-6del
NM_001256864.2(DNAJC6):c.2025G>A (p.Ser675=)
NM_001256864.2(DNAJC6):c.544-20C>T
NM_001256864.2(DNAJC6):c.845G>A (p.Arg282His)

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