ClinVar Miner

List of variants in gene ENO3 reported as benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_001374524.1(ENO3):c.25+467G>A rs73343373
NM_053013.4(ENO3):c.-3+3C>T rs366577
NM_053013.4(ENO3):c.1041C>T (p.Ile347=) rs114208569
NM_053013.4(ENO3):c.1176+8T>C rs111926990
NM_053013.4(ENO3):c.1208G>A (p.Arg403His) rs561474067
NM_053013.4(ENO3):c.1235+3A>G rs73973669
NM_053013.4(ENO3):c.1236-17C>T rs77614413
NM_053013.4(ENO3):c.212A>G (p.Asn71Ser) rs238238
NM_053013.4(ENO3):c.226G>C (p.Ala76Pro) rs143945974
NM_053013.4(ENO3):c.240+17G>A rs75279666
NM_053013.4(ENO3):c.254T>C (p.Val85Ala) rs238239
NM_053013.4(ENO3):c.417G>A (p.Gly139=) rs142390642
NM_053013.4(ENO3):c.788_789insATC (p.Ser263dup) rs548538086
NM_053013.4(ENO3):c.789G>A (p.Ser263=) rs75748087
NM_053013.4(ENO3):c.789G>C (p.Ser263=) rs75748087
NM_053013.4(ENO3):c.828C>T (p.Leu276=) rs35119507
NM_053013.4(ENO3):c.86-10C>T rs201571802
NM_053013.4(ENO3):c.86-3del rs151153333
NM_053013.4(ENO3):c.993C>T (p.Ala331=) rs2230257
NM_053013.4(ENO3):c.994G>A (p.Val332Ile) rs61735456

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