ClinVar Miner

List of variants in gene combination ALDOA, LOC112694756 reported as likely benign for anemia due to erythrocyte enzyme disorder

Included ClinVar conditions (15):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 105
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001243177.4(ALDOA):c.1200C>T (p.Ser400=) rs77290575 0.01088
NM_001243177.4(ALDOA):c.1201G>A (p.Gly401Ser) rs138824667 0.00256
NM_001365304.2(LOC112694756):c.*621+4C>T rs200278984 0.00204
NM_001243177.4(ALDOA):c.648C>G (p.Leu216=) rs112110009 0.00124
NM_001365304.2(LOC112694756):c.*1134-20G>A rs75559164 0.00071
NM_001243177.4(ALDOA):c.471T>A (p.Gly157=) rs142231603 0.00058
NM_001243177.4(ALDOA):c.1182A>G (p.Gln394=) rs143419532 0.00046
NM_001365304.2(LOC112694756):c.*1309-20G>A rs189723657 0.00025
NM_001243177.4(ALDOA):c.426G>A (p.Ala142=) rs772550893 0.00019
NM_001243177.4(ALDOA):c.668A>G (p.Asn223Ser) rs142957871 0.00019
NM_001365304.2(LOC112694756):c.*1308+12A>G rs200733968 0.00014
NM_001243177.4(ALDOA):c.922G>A (p.Val308Ile) rs142759891 0.00013
NM_001365304.2(LOC112694756):c.*622-5C>T rs752764982 0.00008
NM_001243177.4(ALDOA):c.1107C>T (p.Gly369=) rs142315181 0.00006
NM_001243177.4(ALDOA):c.1002G>A (p.Ala334=) rs532473202 0.00005
NM_001243177.4(ALDOA):c.585C>T (p.Asp195=) rs150741747 0.00005
NM_001243177.4(ALDOA):c.312G>A (p.Glu104=) rs779556052 0.00004
NM_001243177.4(ALDOA):c.591T>C (p.Ala197=) rs751360534 0.00004
NM_001243177.4(ALDOA):c.609T>C (p.Arg203=) rs765883841 0.00004
NM_001243177.4(ALDOA):c.921C>T (p.Thr307=) rs148503847 0.00004
NM_001365304.2(LOC112694756):c.*1508+8T>C rs751467136 0.00004
NM_001243177.4(ALDOA):c.945G>C (p.Val315=) rs780658545 0.00003
NM_001365304.2(LOC112694756):c.*834-9C>T rs1057523259 0.00003
NM_001243177.4(ALDOA):c.498C>T (p.Gly166=) rs145811469 0.00002
NM_001243177.4(ALDOA):c.597C>T (p.Phe199=) rs769378422 0.00002
NM_001243177.4(ALDOA):c.1134G>A (p.Ala378=) rs530089317 0.00001
NM_001243177.4(ALDOA):c.1233C>T (p.Leu411=) rs3169548 0.00001
NM_001243177.4(ALDOA):c.309C>T (p.Thr103=) rs758280973 0.00001
NM_001243177.4(ALDOA):c.720C>T (p.Ile240=) rs573479181 0.00001
NM_001243177.4(ALDOA):c.996G>C (p.Glu332Asp) rs565013143 0.00001
NM_001243177.4(ALDOA):c.1008C>T (p.Ile336=)
NM_001243177.4(ALDOA):c.1029G>A (p.Lys343=)
NM_001243177.4(ALDOA):c.1047C>T (p.Pro349=)
NM_001243177.4(ALDOA):c.1080G>A (p.Leu360=)
NM_001243177.4(ALDOA):c.1080G>T (p.Leu360=)
NM_001243177.4(ALDOA):c.1158C>T (p.Ala386=)
NM_001243177.4(ALDOA):c.1224C>T (p.Ser408=)
NM_001243177.4(ALDOA):c.1236C>T (p.Phe412=)
NM_001243177.4(ALDOA):c.1248C>T (p.His416=)
NM_001243177.4(ALDOA):c.1251C>T (p.Ala417=)
NM_001243177.4(ALDOA):c.184C>T (p.Leu62=)
NM_001243177.4(ALDOA):c.189C>T (p.Thr63=)
NM_001243177.4(ALDOA):c.288G>A (p.Lys96=)
NM_001243177.4(ALDOA):c.318C>T (p.Thr106=)
NM_001243177.4(ALDOA):c.364G>A (p.Asp122Asn)
NM_001243177.4(ALDOA):c.396C>T (p.Ile132=)
NM_001243177.4(ALDOA):c.408G>A (p.Glu136=)
NM_001243177.4(ALDOA):c.423G>A (p.Lys141=)
NM_001243177.4(ALDOA):c.447C>T (p.Pro149=)
NM_001243177.4(ALDOA):c.462C>T (p.Ser154=)
NM_001243177.4(ALDOA):c.525C>T (p.Gly175=)
NM_001243177.4(ALDOA):c.552G>C (p.Gly184=)
NM_001243177.4(ALDOA):c.576C>T (p.Tyr192=)
NM_001243177.4(ALDOA):c.582G>A (p.Lys194=)
NM_001243177.4(ALDOA):c.588A>C (p.Gly196=)
NM_001243177.4(ALDOA):c.630A>G (p.Glu210=)
NM_001243177.4(ALDOA):c.636C>T (p.Thr212=)
NM_001243177.4(ALDOA):c.684T>C (p.Tyr228=) rs1596813728
NM_001243177.4(ALDOA):c.729T>C (p.Pro243=)
NM_001243177.4(ALDOA):c.780C>T (p.Thr260=)
NM_001243177.4(ALDOA):c.804C>T (p.Tyr268=)
NM_001243177.4(ALDOA):c.828C>T (p.Ile276=)
NM_001243177.4(ALDOA):c.867C>T (p.Thr289=)
NM_001243177.4(ALDOA):c.900T>C (p.His300=)
NM_001243177.4(ALDOA):c.912C>T (p.Ala304=)
NM_001243177.4(ALDOA):c.918G>A (p.Ala306=)
NM_001243177.4(ALDOA):c.951C>A (p.Pro317=)
NM_001243177.4(ALDOA):c.963G>C (p.Gly321=)
NM_001243177.4(ALDOA):c.966C>T (p.Ile322=)
NM_001365304.2(LOC112694756):c.*1049+12G>A
NM_001365304.2(LOC112694756):c.*1049+17T>C
NM_001365304.2(LOC112694756):c.*1049+20A>G
NM_001365304.2(LOC112694756):c.*1049+7C>T
NM_001365304.2(LOC112694756):c.*1049+8T>C
NM_001365304.2(LOC112694756):c.*1050-10C>T
NM_001365304.2(LOC112694756):c.*1050-12C>T
NM_001365304.2(LOC112694756):c.*1050-7C>T
NM_001365304.2(LOC112694756):c.*1050-9G>A
NM_001365304.2(LOC112694756):c.*1133+11A>G
NM_001365304.2(LOC112694756):c.*1134-12G>C
NM_001365304.2(LOC112694756):c.*1134-17C>T
NM_001365304.2(LOC112694756):c.*1134-4C>T
NM_001365304.2(LOC112694756):c.*1308+15C>T
NM_001365304.2(LOC112694756):c.*1309-7T>G
NM_001365304.2(LOC112694756):c.*1309-8C>T
NM_001365304.2(LOC112694756):c.*1508+9A>T
NM_001365304.2(LOC112694756):c.*1508+9_*1508+19dup
NM_001365304.2(LOC112694756):c.*1509-11T>C
NM_001365304.2(LOC112694756):c.*1509-14C>A
NM_001365304.2(LOC112694756):c.*1509-14C>T
NM_001365304.2(LOC112694756):c.*1509-16C>T
NM_001365304.2(LOC112694756):c.*1509-17C>T
NM_001365304.2(LOC112694756):c.*1509-18A>T
NM_001365304.2(LOC112694756):c.*622-11G>C
NM_001365304.2(LOC112694756):c.*622-15A>G
NM_001365304.2(LOC112694756):c.*622-3del
NM_001365304.2(LOC112694756):c.*833+10G>A
NM_001365304.2(LOC112694756):c.*833+16C>T
NM_001365304.2(LOC112694756):c.*833+17C>T
NM_001365304.2(LOC112694756):c.*833+18G>A
NM_001365304.2(LOC112694756):c.*833+19G>A
NM_001365304.2(LOC112694756):c.*833+9A>C
NM_001365304.2(LOC112694756):c.*834-14C>T
NM_001365304.2(LOC112694756):c.*834-19G>A
NM_001365304.2(LOC112694756):c.*888+8C>T

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.