ClinVar Miner

List of variants in gene HNRNPA2B1 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002137.4(HNRNPA2B1):c.965-170A>G rs12672536 0.15316
NM_002137.4(HNRNPA2B1):c.519A>G (p.Arg173=) rs34317198 0.04885
NM_002137.4(HNRNPA2B1):c.964+288T>C rs2070601 0.04841
NM_002137.4(HNRNPA2B1):c.7-340C>T rs10255851 0.04529
NM_002137.4(HNRNPA2B1):c.117+4T>C rs41275982 0.03091
NM_002137.4(HNRNPA2B1):c.721+54C>T rs75904946 0.03057
NM_002137.4(HNRNPA2B1):c.7-257T>G rs11971308 0.03034
NM_002137.4(HNRNPA2B1):c.265-52T>C rs73281546 0.03032
NM_002137.4(HNRNPA2B1):c.965-199A>G rs56276467 0.02933
NM_002137.4(HNRNPA2B1):c.964+244A>C rs56132015 0.02932
NM_002137.4(HNRNPA2B1):c.659-108C>T rs61009175 0.02930
NM_002137.4(HNRNPA2B1):c.265-141A>T rs73281548 0.02827
NM_002137.4(HNRNPA2B1):c.722-277A>G rs76558212 0.01894
NC_000007.14:g.26200944C>G rs79503307 0.01085
NM_002137.4(HNRNPA2B1):c.964+64_964+68del rs56684003 0.01024
NM_002137.4(HNRNPA2B1):c.264+66dup rs144507429 0.00809
NM_002137.4(HNRNPA2B1):c.841+6A>G rs144309126 0.00625
NM_002137.4(HNRNPA2B1):c.722-194T>G rs116376035 0.00559
NM_002137.4(HNRNPA2B1):c.645T>C (p.Phe215=) rs117082250 0.00481
NM_002137.4(HNRNPA2B1):c.264+33A>G rs116289690 0.00449
NM_002137.4(HNRNPA2B1):c.-97C>G rs141936134 0.00388
NM_002137.4(HNRNPA2B1):c.288T>C (p.His96=) rs142061533 0.00214
NM_002137.4(HNRNPA2B1):c.7-456T>C rs561550234 0.00168
NM_002137.4(HNRNPA2B1):c.756A>C (p.Gly252=) rs199909637 0.00022
NM_002137.4(HNRNPA2B1):c.*4T>G rs200301894 0.00021
NM_002137.4(HNRNPA2B1):c.866A>G (p.Asn289Ser) rs911715553 0.00001
NM_002137.4(HNRNPA2B1):c.943A>G (p.Met315Val) rs372687249 0.00001
NM_002137.4(HNRNPA2B1):c.-131C>G rs146346849
NM_002137.4(HNRNPA2B1):c.265-119A>T rs17153396
NM_002137.4(HNRNPA2B1):c.475+65C>G rs73683262
NM_002137.4(HNRNPA2B1):c.476-62del rs373381657
NM_002137.4(HNRNPA2B1):c.6+191_6+196del rs538696426
NM_002137.4(HNRNPA2B1):c.659-65_659-64dup rs111941879
NM_002137.4(HNRNPA2B1):c.659-7C>G rs199606705
NM_002137.4(HNRNPA2B1):c.7-133A>G
NM_002137.4(HNRNPA2B1):c.7-289_7-286del rs71953553
NM_002137.4(HNRNPA2B1):c.7-297del rs199985423
NM_002137.4(HNRNPA2B1):c.7-297dup rs199985423
NM_002137.4(HNRNPA2B1):c.7-298_7-297del rs199985423
NM_002137.4(HNRNPA2B1):c.7-326_7-323del rs145309516
NM_002137.4(HNRNPA2B1):c.721+123G>T rs17796710
NM_002137.4(HNRNPA2B1):c.722-336T>G rs4722589
NM_002137.4(HNRNPA2B1):c.724G>T (p.Gly242Cys) rs1783162945
NM_002137.4(HNRNPA2B1):c.797A>G (p.Asn266Ser) rs1554331125
NM_002137.4(HNRNPA2B1):c.964+269C>A rs114142296
NM_002137.4(HNRNPA2B1):c.965-264T>G rs58068323

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.