ClinVar Miner

List of variants in gene OFD1 reported as benign for not provided

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Gene type:
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Total variants: 52
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HGVS dbSNP gnomAD frequency
NM_003611.3(OFD1):c.2261-80G>A rs6527959 0.36225
NM_003611.3(OFD1):c.1130-272A>G rs2074099 0.28441
NM_003611.3(OFD1):c.1129+234A>G rs73633577 0.28098
NM_003611.3(OFD1):c.1129+16A>G rs3815049 0.28069
NM_003611.3(OFD1):c.655-140G>C rs16992216 0.04133
NM_003611.3(OFD1):c.828+51G>A rs17311049 0.02375
NM_003611.3(OFD1):c.2387+11C>T rs140369491 0.02280
NM_003611.3(OFD1):c.112-63C>T rs142075256 0.02252
NM_003611.3(OFD1):c.935+663C>T rs139868392 0.02235
NM_003611.3(OFD1):c.312+206G>T rs59650333 0.02134
NM_003611.3(OFD1):c.935+518A>G rs139186459 0.02004
NM_003611.3(OFD1):c.935+636A>G rs9699014 0.01595
NM_003611.3(OFD1):c.1655-189A>G rs7058591 0.01592
NM_003611.3(OFD1):c.1055+264A>G rs187960773 0.01560
NM_003611.3(OFD1):c.1412-75dup rs200184687 0.01557
NM_003611.3(OFD1):c.2387+249C>A rs16979184 0.01536
NM_003611.3(OFD1):c.1020G>A (p.Glu340=) rs5979959 0.00630
NM_003611.3(OFD1):c.2929-18C>T rs180940027 0.00601
NM_003611.3(OFD1):c.1264A>G (p.Lys422Glu) rs61746932 0.00584
NM_003611.3(OFD1):c.1542+21G>A rs16979182 0.00425
NM_003611.3(OFD1):c.2663A>C (p.Lys888Thr) rs149647255 0.00381
NM_003611.3(OFD1):c.1923G>A (p.Glu641=) rs145300245 0.00298
NM_003611.3(OFD1):c.2388-38A>G rs140196295 0.00296
NM_003611.3(OFD1):c.1655-89T>C rs750444669 0.00235
NM_003611.3(OFD1):c.2044A>C (p.Ile682Leu) rs148239437 0.00227
NM_003611.3(OFD1):c.2599+34G>A rs191772761 0.00206
NM_003611.3(OFD1):c.2033C>G (p.Ala678Gly) rs143954823 0.00187
NM_003611.3(OFD1):c.1654+8A>G rs200767363 0.00184
NM_003611.3(OFD1):c.655-32G>C rs191310440 0.00122
NM_003611.3(OFD1):c.*3A>G rs183202009 0.00113
NM_003611.3(OFD1):c.381+27A>G rs375363601 0.00082
NM_003611.3(OFD1):c.654+41T>C rs370365975 0.00055
NM_003611.3(OFD1):c.2524G>A (p.Gly842Arg) rs146047094 0.00023
NM_003611.3(OFD1):c.476T>C (p.Met159Thr) rs141708295 0.00009
NM_003611.3(OFD1):c.2260+8A>G rs768452237 0.00007
NM_003611.3(OFD1):c.2482T>G (p.Phe828Val) rs779051357 0.00003
NM_003611.3(OFD1):c.2117C>T (p.Thr706Ile) rs773224811 0.00001
NM_003611.3(OFD1):c.*47G>A rs202080584
NM_003611.3(OFD1):c.1055+118del rs3214141
NM_003611.3(OFD1):c.112-172del rs3214140
NM_003611.3(OFD1):c.1130-175C>T rs16999063
NM_003611.3(OFD1):c.1412-11del rs36052228
NM_003611.3(OFD1):c.2052C>G (p.Ser684=) rs61742891
NM_003611.3(OFD1):c.2052C>T (p.Ser684=) rs61742891
NM_003611.3(OFD1):c.2387+90_2387+91dup rs112117780
NM_003611.3(OFD1):c.2387+91dup rs112117780
NM_003611.3(OFD1):c.2757+163dup rs202238503
NM_003611.3(OFD1):c.412+282dup rs751700372
NM_003611.3(OFD1):c.829-280del rs57776230
NM_003611.3(OFD1):c.829-287del rs35839446
NM_003611.3(OFD1):c.829-287dup rs35839446
NM_003611.3(OFD1):c.935+66A>G rs7878592

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