ClinVar Miner

List of variants reported as benign for Axenfeld-Rieger syndrome by Illumina Laboratory Services, Illumina

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_153427.2(PITX2):c.-1068C>T rs62338989 0.17862
NM_000325.6(PITX2):c.*454C>T rs6533526 0.05143
NM_000325.6(PITX2):c.*471G>A rs75911264 0.01337
NM_153427.2(PITX2):c.-392G>T rs113778706 0.01298
NM_000325.6(PITX2):c.618T>G (p.Ser206=) rs35946364 0.01175
NM_153427.3(PITX2):c.46+8C>G rs199896960 0.01041
NM_153427.3(PITX2):c.-211G>A rs111733107 0.00270
NM_000325.6(PITX2):c.562G>A (p.Ala188Thr) rs77144743 0.00264
NM_153427.2(PITX2):c.-362C>G rs181197472 0.00251
NM_153427.2(PITX2):c.-1024G>A rs181439547 0.00231
NM_153427.2(PITX2):c.-1111C>G rs187210297 0.00231
NM_153427.2(PITX2):c.-1335C>A rs145638916 0.00177
NM_153427.2(PITX2):c.-793C>A rs145044365 0.00165
NM_000325.6(PITX2):c.819G>A (p.Pro273=) rs148191851 0.00135
NM_000325.6(PITX2):c.862C>T (p.Leu288=) rs139401187 0.00035
NM_153427.2(PITX2):c.-1311G>T rs192250966 0.00030
NM_000325.6(PITX2):c.639A>T (p.Ser213=) rs141176394 0.00029
NM_153427.2(PITX2):c.-967C>T rs368647502 0.00024
NM_000325.6(PITX2):c.619A>G (p.Met207Val) rs138163892 0.00023
NM_153427.3(PITX2):c.-79G>A rs535056127 0.00012
NM_001204398.1(PITX2):c.-11+12T>C rs140614517 0.00009
NM_000325.6(PITX2):c.*340A>G rs551209662
NM_000325.6(PITX2):c.224A>C (p.Gln75Pro) rs201628949
NM_153427.2(PITX2):c.-1532C>A rs117231596
NM_153427.2(PITX2):c.-485C>G rs2739200

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