ClinVar Miner

List of variants in gene ANK1 reported as benign for anemia (disease)

Included ClinVar conditions (281):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_000037.4(ANK1):c.*1402G>T rs116137861
NM_000037.4(ANK1):c.*1609C>G rs78203311
NM_000037.4(ANK1):c.*1899G>A rs72638943
NM_000037.4(ANK1):c.*2022G>A rs112447985
NM_000037.4(ANK1):c.*2152T>G rs543817
NM_000037.4(ANK1):c.*238T>C rs72638944
NM_000037.4(ANK1):c.*36+989dup rs59908561
NM_000037.4(ANK1):c.*774A>G rs142696529
NM_000037.4(ANK1):c.1320G>A (p.Pro440=) rs28533718
NM_000037.4(ANK1):c.1590C>T (p.Ala530=) rs61758865
NM_000037.4(ANK1):c.1782C>A (p.Ser594=) rs61753679
NM_000037.4(ANK1):c.183G>C (p.Val61=) rs61753680
NM_000037.4(ANK1):c.1856G>A (p.Arg619His) rs2304877
NM_000037.4(ANK1):c.2073C>T (p.Gly691=) rs1137177
NM_000037.4(ANK1):c.2211C>G (p.Pro737=) rs34194642
NM_000037.4(ANK1):c.2349C>T (p.Thr783=) rs2304880
NM_000037.4(ANK1):c.237C>T (p.Asn79=) rs372696694
NM_000037.4(ANK1):c.2495G>A (p.Arg832Gln) rs34523608
NM_000037.4(ANK1):c.2913G>C (p.Leu971=) rs504574
NM_000037.4(ANK1):c.3033C>T (p.Ser1011=) rs61758866
NM_000037.4(ANK1):c.3115+9G>A rs150850103
NM_000037.4(ANK1):c.315C>T (p.Asn105=) rs2304871
NM_000037.4(ANK1):c.3224C>T (p.Thr1075Ile) rs35213384
NM_000037.4(ANK1):c.3486C>T (p.Ser1162=) rs35964634
NM_000037.4(ANK1):c.3668T>C (p.Val1223Ala) rs185516533
NM_000037.4(ANK1):c.3813G>A (p.Glu1271=) rs16890758
NM_000037.4(ANK1):c.3973A>G (p.Met1325Val) rs10093583
NM_000037.4(ANK1):c.4008G>A (p.Pro1336=) rs147536061
NM_000037.4(ANK1):c.4101C>T (p.Ala1367=) rs7816734
NM_000037.4(ANK1):c.4385C>T (p.Ala1462Val) rs34664882
NM_000037.4(ANK1):c.4506C>T (p.Arg1502=) rs34265667
NM_000037.4(ANK1):c.450A>G (p.Val150=) rs6982971
NM_000037.4(ANK1):c.489C>T (p.Leu163=) rs34173100
NM_000037.4(ANK1):c.499G>C (p.Gly167Arg) rs201024919
NM_000037.4(ANK1):c.5096+16T>C rs508112
NM_000037.4(ANK1):c.5265G>A (p.Val1755=) rs750625
NM_000037.4(ANK1):c.5395-1147C>G rs112350393
NM_000037.4(ANK1):c.5479-3T>C rs515071
NM_000037.4(ANK1):c.5544+91C>T rs72638959
NM_000037.4(ANK1):c.597G>A (p.Pro199=) rs2304873
NM_000037.4(ANK1):c.612+18G>C rs57815524
NM_000037.4(ANK1):c.654C>A (p.Asn218Lys) rs61735313
NM_000037.4(ANK1):c.675C>T (p.Leu225=) rs146507999
NM_000037.4(ANK1):c.909+7A>G rs17661203
NM_001142446.2(ANK1):c.127-39509T>C rs77173848

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