ClinVar Miner

List of variants in gene LPIN2 reported as likely benign for anemia (disease)

Included ClinVar conditions (262):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP
NM_014646.2(LPIN2):c.*1052T>C rs59566682
NM_014646.2(LPIN2):c.*1691A>G rs112588494
NM_014646.2(LPIN2):c.*2197_*2198delTT rs55834965
NM_014646.2(LPIN2):c.*2241T>C rs16944033
NM_014646.2(LPIN2):c.*2493C>G rs8091401
NM_014646.2(LPIN2):c.*2822C>T rs73375246
NM_014646.2(LPIN2):c.*2923C>T rs202079191
NM_014646.2(LPIN2):c.*2924delC rs148191039
NM_014646.2(LPIN2):c.*2946G>A rs4781
NM_014646.2(LPIN2):c.*501T>C rs35176958
NM_014646.2(LPIN2):c.*557G>A rs112795993
NM_014646.2(LPIN2):c.*637G>A rs118142692
NM_014646.2(LPIN2):c.*723A>G rs76325993
NM_014646.2(LPIN2):c.*797T>G rs3810064
NM_014646.2(LPIN2):c.*950A>C rs3810065
NM_014646.2(LPIN2):c.*99C>T rs143728428
NM_014646.2(LPIN2):c.-36C>G rs58940048
NM_014646.2(LPIN2):c.-37C>G rs59096963
NM_014646.2(LPIN2):c.1168+11G>C rs79439091
NM_014646.2(LPIN2):c.1169-7delT rs746626720
NM_014646.2(LPIN2):c.1329C>A (p.Ser443=) rs759651506
NM_014646.2(LPIN2):c.1510C>T (p.Leu504Phe) rs104895500
NM_014646.2(LPIN2):c.1735T>C (p.Ser579Pro) rs150022314
NM_014646.2(LPIN2):c.1800C>T (p.Ala600=) rs369572309
NM_014646.2(LPIN2):c.2316C>A (p.Ser772=) rs145270447
NM_014646.2(LPIN2):c.2371C>T (p.Leu791=) rs373520277
NM_014646.2(LPIN2):c.2443-9C>T rs191749331
NM_014646.2(LPIN2):c.2583C>T (p.Phe861=) rs141043192
NM_014646.2(LPIN2):c.2671G>A (p.Asp891Asn) rs200648652
NM_014646.2(LPIN2):c.582G>A (p.Gln194=) rs1555677025
NM_014646.2(LPIN2):c.608C>T (p.Ser203Phe) rs144555528
NM_014646.2(LPIN2):c.87G>A (p.Gly29=) rs1346313879
NM_014646.2(LPIN2):c.991G>T (p.Ala331Ser) rs80338805

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