ClinVar Miner

List of variants in gene GLI2 reported as likely benign for Holoprosencephaly sequence

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Gene type:
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Total variants: 35
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HGVS dbSNP
NM_005270.4(GLI2):c.*1147_*1148delAT rs199943079
NM_005270.4(GLI2):c.*118C>T rs190824141
NM_005270.4(GLI2):c.*1375A>C rs200730065
NM_005270.4(GLI2):c.*1785A>G rs150539352
NM_005270.4(GLI2):c.*1826T>G rs139459477
NM_005270.4(GLI2):c.*419C>T rs370777016
NM_005270.4(GLI2):c.*42C>T rs185228238
NM_005270.4(GLI2):c.*569T>A rs75544832
NM_005270.4(GLI2):c.-1G>C rs369138377
NM_005270.4(GLI2):c.-7G>A rs112131051
NM_005270.4(GLI2):c.1294G>A (p.Val432Met) rs142296407
NM_005270.4(GLI2):c.148+14C>T rs190309269
NM_005270.4(GLI2):c.1761G>A (p.Thr587=) rs61732852
NM_005270.4(GLI2):c.1802A>G (p.Asn601Ser) rs61732851
NM_005270.4(GLI2):c.1859C>T (p.Thr620Met) rs142775128
NM_005270.4(GLI2):c.1869C>A (p.Gly623=) rs61732850
NM_005270.4(GLI2):c.1944C>T (p.Thr648=) rs13008360
NM_005270.4(GLI2):c.1986G>A (p.Ser662=) rs114259687
NM_005270.4(GLI2):c.2088A>G (p.Ala696=) rs146059306
NM_005270.4(GLI2):c.2916T>A (p.Pro972=) rs747247646
NM_005270.4(GLI2):c.2940C>T (p.Ser980=) rs146811565
NM_005270.4(GLI2):c.3018C>T (p.Gly1006=) rs373880077
NM_005270.4(GLI2):c.3048C>T (p.Asp1016=) rs140479803
NM_005270.4(GLI2):c.3349G>T (p.Val1117Leu) rs147580961
NM_005270.4(GLI2):c.3590G>A (p.Gly1197Asp) rs114823319
NM_005270.4(GLI2):c.3882G>A (p.Thr1294=) rs115052795
NM_005270.4(GLI2):c.3943C>T (p.Pro1315Ser) rs114376238
NM_005270.4(GLI2):c.4054A>G (p.Met1352Val) rs149140724
NM_005270.4(GLI2):c.4207A>G (p.Met1403Val) rs577126364
NM_005270.4(GLI2):c.4332G>A (p.Met1444Ile) rs146467786
NM_005270.4(GLI2):c.4333C>T (p.Leu1445Phe) rs146207623
NM_005270.4(GLI2):c.4558G>A (p.Asp1520Asn) rs114814747
NM_005270.4(GLI2):c.4663T>C (p.Ser1555Pro) rs144372453
NM_005270.4(GLI2):c.720C>T (p.Asp240=) rs142793481
NM_005270.4(GLI2):c.963C>G (p.Pro321=) rs149894186

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