ClinVar Miner

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

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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_003611.3(OFD1):c.2387+11C>T rs140369491 0.02280
NM_003611.3(OFD1):c.2758-53A>C rs144401718 0.02254
NM_003611.3(OFD1):c.1412-411G>A rs6633319 0.01656
NM_003611.3(OFD1):c.829-287A>T rs761965435 0.01579
NM_003611.3(OFD1):c.2489-90G>A rs16979187 0.01532
NM_003611.3(OFD1):c.829-254G>T rs141380452 0.01515
NM_003611.3(OFD1):c.2997-29A>G rs148787280 0.01335
NM_003611.3(OFD1):c.1411+240C>T rs151068148 0.01334
NM_003611.3(OFD1):c.*123T>G rs182746098 0.01246
NM_003611.3(OFD1):c.1129+208A>G rs143221184 0.00964
NM_003611.3(OFD1):c.2260+160C>G rs151255070 0.00887
NM_003611.3(OFD1):c.412+281A>C rs116542198 0.00871
NM_003611.3(OFD1):c.517+298C>G rs143016744 0.00755
NM_003611.3(OFD1):c.2388-188A>T rs147342417 0.00716
NM_003611.3(OFD1):c.313-175A>G rs185739141 0.00701
NM_003611.3(OFD1):c.2996+81T>C rs190979841 0.00683
NM_003611.3(OFD1):c.1654+191T>G rs138721221 0.00641
NM_003611.3(OFD1):c.714T>C (p.Tyr238=) rs139848884 0.00637
NM_003611.3(OFD1):c.1654+336G>A rs141147258 0.00617
NM_003611.3(OFD1):c.413-263G>A rs148137087 0.00440
NM_003611.3(OFD1):c.2757+52C>T rs189935382 0.00301
NM_003611.3(OFD1):c.1923G>A (p.Glu641=) rs145300245 0.00298
NM_003611.3(OFD1):c.517+20T>C rs139112266 0.00200
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.2261-24G>A rs146759174 0.00176
NM_003611.3(OFD1):c.2996+34A>C rs373123585 0.00128
NM_003611.3(OFD1):c.2398A>G (p.Arg800Gly) rs139406798 0.00049
NM_003611.3(OFD1):c.1654+9C>T rs200007045 0.00044
NM_003611.3(OFD1):c.1543-19C>G rs201761130 0.00041
NM_003611.3(OFD1):c.2376G>A (p.Glu792=) rs183241931 0.00026
NM_003611.3(OFD1):c.1294A>G (p.Lys432Glu) rs142352920 0.00024
NM_003611.3(OFD1):c.1129+8T>A rs199572133 0.00023
NM_003611.3(OFD1):c.2260+12G>A rs375507459 0.00023
NM_003611.3(OFD1):c.1730A>G (p.Asn577Ser) rs200465596 0.00017
NM_003611.3(OFD1):c.2235C>T (p.Ser745=) rs372503752 0.00015
NM_003611.3(OFD1):c.2060C>T (p.Pro687Leu) rs146251034 0.00013
NM_003611.3(OFD1):c.1536A>G (p.Gln512=) rs138532127 0.00011
NM_003611.3(OFD1):c.936-2A>G rs199902986 0.00011
NM_003611.3(OFD1):c.935+12A>G rs199773671 0.00010
NM_003611.3(OFD1):c.2260+8A>G rs768452237 0.00007
NM_003611.3(OFD1):c.2319A>G (p.Pro773=) rs752137789 0.00007
NM_003611.3(OFD1):c.1634A>G (p.Gln545Arg) rs373792491 0.00006
NM_003611.3(OFD1):c.1930C>T (p.Arg644Cys) rs185831378 0.00006
NM_003611.3(OFD1):c.2139C>T (p.Val713=) rs764423950 0.00006
NM_003611.3(OFD1):c.1347A>G (p.Ala449=) rs151287373 0.00005
NM_003611.3(OFD1):c.858G>A (p.Arg286=) rs778507612 0.00005
NM_003611.3(OFD1):c.1694T>C (p.Val565Ala) rs529916753 0.00003
NM_003611.3(OFD1):c.1926C>T (p.Ala642=) rs757775981 0.00003
NM_003611.3(OFD1):c.1400G>A (p.Arg467His) rs375577267 0.00002
NM_003611.3(OFD1):c.2078G>A (p.Gly693Glu) rs754615597 0.00002
NM_003611.3(OFD1):c.1719A>G (p.Leu573=) rs1186088715 0.00001
NM_003611.3(OFD1):c.2136C>T (p.Asp712=) rs775705991 0.00001
NM_003611.3(OFD1):c.2289C>A (p.Pro763=) rs947500861 0.00001
NM_003611.3(OFD1):c.1055+187C>G rs190715863
NM_003611.3(OFD1):c.1055+214C>A rs151120669
NM_003611.3(OFD1):c.126C>T (p.Asn42=)
NM_003611.3(OFD1):c.1412-5C>T rs1235401479
NM_003611.3(OFD1):c.1412-8C>T rs764992175
NM_003611.3(OFD1):c.1425G>T (p.Pro475=)
NM_003611.3(OFD1):c.1543-147dup rs201339023
NM_003611.3(OFD1):c.1803A>G (p.Ala601=) rs770394963
NM_003611.3(OFD1):c.1944T>C (p.Ala648=)
NM_003611.3(OFD1):c.2052C>G (p.Ser684=) rs61742891
NM_003611.3(OFD1):c.2929-42C>A
NM_003611.3(OFD1):c.412+264C>A rs868585834
NM_003611.3(OFD1):c.412+282del rs751700372
NM_003611.3(OFD1):c.935+595A>G
NM_003611.3(OFD1):c.935+628T>C

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