ClinVar Miner

List of variants in gene HNRNPA2B1 reported as benign for hereditary dementia

Included ClinVar conditions (231):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_002137.4(HNRNPA2B1):c.519A>G (p.Arg173=) rs34317198 0.04885
NM_002137.4(HNRNPA2B1):c.117+4T>C rs41275982 0.03091
NM_002137.4(HNRNPA2B1):c.841+6A>G rs144309126 0.00625
NM_002137.4(HNRNPA2B1):c.645T>C (p.Phe215=) rs117082250 0.00481
NM_002137.4(HNRNPA2B1):c.721+19T>C rs183451681 0.00296
NM_002137.4(HNRNPA2B1):c.288T>C (p.His96=) rs142061533 0.00214
NM_002137.4(HNRNPA2B1):c.658+18C>T rs200943057 0.00103
NM_002137.4(HNRNPA2B1):c.964+10A>G rs181705411 0.00058
NM_002137.4(HNRNPA2B1):c.117+13C>T rs201523113 0.00052
NM_002137.4(HNRNPA2B1):c.243A>G (p.Pro81=) rs143134057 0.00043
NM_002137.4(HNRNPA2B1):c.906T>A (p.Gly302=) rs139270847 0.00037
NM_002137.4(HNRNPA2B1):c.475+9C>T rs199612730 0.00006
NM_002137.4(HNRNPA2B1):c.659-19T>C rs781454007 0.00004
NM_002137.4(HNRNPA2B1):c.476-16G>A rs546524344
NM_002137.4(HNRNPA2B1):c.659-13del
NM_002137.4(HNRNPA2B1):c.659-13dup rs754016775
NM_002137.4(HNRNPA2B1):c.659-14_659-13del rs754016775
NM_002137.4(HNRNPA2B1):c.659-7C>G rs199606705
NM_002137.4(HNRNPA2B1):c.7-137del rs759915055
NM_002137.4(HNRNPA2B1):c.7-143del rs57800062
NM_002137.4(HNRNPA2B1):c.7-143dup
NM_002137.4(HNRNPA2B1):c.7-145_7-143del
NM_002137.4(HNRNPA2B1):c.842-11dup rs1465279377

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