ClinVar Miner

List of variants in gene ANKRD26 reported as likely benign for blood platelet disease

Included ClinVar conditions (105):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_014915.3(ANKRD26):c.*815dup rs397845107 0.10151
NM_014915.3(ANKRD26):c.*1235del rs112091269 0.08856
NM_014915.3(ANKRD26):c.*68_*69del rs3215884 0.08761
NM_014915.3(ANKRD26):c.3655G>A (p.Val1219Ile) rs146819984 0.00781
NM_014915.3(ANKRD26):c.2679A>G (p.Gln893=) rs61730098 0.00215
NM_014915.3(ANKRD26):c.3007G>A (p.Glu1003Lys) rs41304587 0.00141
NM_014915.3(ANKRD26):c.1635+9T>C rs199590440 0.00016
NM_014915.3(ANKRD26):c.5060A>T (p.Asn1687Ile) rs373138646 0.00009
NM_014915.3(ANKRD26):c.1213A>G (p.Met405Val) rs555822164 0.00006
NM_014915.3(ANKRD26):c.269A>G (p.Asn90Ser) rs752629436 0.00005
NM_014915.3(ANKRD26):c.1565-4T>C rs747570982 0.00004
NM_014915.3(ANKRD26):c.452A>C (p.His151Pro) rs752031374 0.00003
NM_014915.3(ANKRD26):c.3367A>G (p.Asn1123Asp) rs746125031 0.00002
NM_014915.3(ANKRD26):c.3704A>T (p.Gln1235Leu) rs765506121 0.00002
NM_014915.3(ANKRD26):c.2642A>G (p.Asn881Ser) rs926871139 0.00001
NM_014915.3(ANKRD26):c.-51T>A rs762195334
NM_014915.3(ANKRD26):c.1364A>G (p.Asp455Gly) rs199857139
NM_014915.3(ANKRD26):c.1590AGA[2] (p.Glu533del) rs138423863
NM_014915.3(ANKRD26):c.1986-3del rs113123391
NM_014915.3(ANKRD26):c.937G>A (p.Asp313Asn) rs61730102

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