ClinVar Miner

List of variants in gene combination BBS1, ZDHHC24 reported as uncertain significance for Bardet-Biedl syndrome

Included ClinVar conditions (37):
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Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP
NM_024649.5(BBS1):c.*104G>C rs554182779
NM_024649.5(BBS1):c.*1088G>A rs886048531
NM_024649.5(BBS1):c.*10T>A rs765633556
NM_024649.5(BBS1):c.*1217C>A
NM_024649.5(BBS1):c.*1274A>G
NM_024649.5(BBS1):c.*1349T>C
NM_024649.5(BBS1):c.*259C>A
NM_024649.5(BBS1):c.*473C>T rs886048526
NM_024649.5(BBS1):c.*474G>A
NM_024649.5(BBS1):c.*514C>T rs886048527
NM_024649.5(BBS1):c.*51C>G
NM_024649.5(BBS1):c.*522C>T rs886048528
NM_024649.5(BBS1):c.*562_*563dup rs886048529
NM_024649.5(BBS1):c.*776G>A
NM_024649.5(BBS1):c.*855G>A rs886048530
NM_024649.5(BBS1):c.*886C>T
NM_024649.5(BBS1):c.*950C>T
NM_024649.5(BBS1):c.1016A>T (p.His339Leu) rs1389335279
NM_024649.5(BBS1):c.1061A>G (p.Glu354Gly) rs1555048530
NM_024649.5(BBS1):c.1071T>C (p.Ile357=)
NM_024649.5(BBS1):c.1088T>C (p.Leu363Pro) rs540217506
NM_024649.5(BBS1):c.1109C>T (p.Pro370Leu)
NM_024649.5(BBS1):c.1110+15C>T rs371084544
NM_024649.5(BBS1):c.1110G>A (p.Pro370=) rs183771956
NM_024649.5(BBS1):c.1138C>T (p.Arg380Trp) rs752299442
NM_024649.5(BBS1):c.1139G>A (p.Arg380Gln) rs758139447
NM_024649.5(BBS1):c.1155C>G (p.Asp385Glu)
NM_024649.5(BBS1):c.1180+5G>A rs886048525
NM_024649.5(BBS1):c.1194C>A (p.Ile398=) rs200577824
NM_024649.5(BBS1):c.1243G>A (p.Val415Met)
NM_024649.5(BBS1):c.1264G>A (p.Ala422Thr)
NM_024649.5(BBS1):c.1277A>G (p.Asn426Ser) rs755782127
NM_024649.5(BBS1):c.1310A>T (p.Gln437Leu)
NM_024649.5(BBS1):c.1334G>C (p.Gly445Ala) rs765829383
NM_024649.5(BBS1):c.1338C>T (p.Thr446=) rs368302072
NM_024649.5(BBS1):c.1339G>A (p.Ala447Thr) rs200116631
NM_024649.5(BBS1):c.1371C>T (p.Tyr457=)
NM_024649.5(BBS1):c.1383A>G (p.Leu461=) rs557739576
NM_024649.5(BBS1):c.1394G>A (p.Arg465His) rs146072788
NM_024649.5(BBS1):c.1439C>A (p.Thr480Lys) rs374706769
NM_024649.5(BBS1):c.1535G>A (p.Arg512His) rs202205304
NM_024649.5(BBS1):c.1553T>C (p.Leu518Pro) rs121917778
NM_024649.5(BBS1):c.1565T>C (p.Leu522Pro)
NM_024649.5(BBS1):c.1570_1572del (p.Asn524del) rs863224782
NM_024649.5(BBS1):c.1585T>G (p.Ser529Ala) rs1316472200
NM_024649.5(BBS1):c.1592C>T (p.Pro531Leu)
NM_024649.5(BBS1):c.1594C>T (p.Arg532Trp) rs770105141
NM_024649.5(BBS1):c.1595G>A (p.Arg532Gln) rs142648652
NM_024649.5(BBS1):c.1595G>T (p.Arg532Leu)
NM_024649.5(BBS1):c.1631T>A (p.Leu544His) rs1555050401
NM_024649.5(BBS1):c.1634A>G (p.Asn545Ser) rs148948642
NM_024649.5(BBS1):c.1676G>A (p.Gly559Asp)
NM_024649.5(BBS1):c.1676_1678del (p.Gly559_Ile560delinsVal) rs1555050422
NM_024649.5(BBS1):c.1695G>A (p.Lys565=) rs1555050427
NM_024649.5(BBS1):c.1702G>A (p.Val568Met) rs754300140
NM_024649.5(BBS1):c.1709G>A (p.Arg570Gln)
NM_024649.5(BBS1):c.1717C>T (p.Gln573Ter) rs1450045618
NM_024649.5(BBS1):c.1744G>A (p.Val582Ile) rs111358560
NM_024649.5(BBS1):c.1762G>A (p.Glu588Lys) rs761304709
NM_024649.5(BBS1):c.726G>A (p.Met242Ile) rs773588060
NM_024649.5(BBS1):c.739G>A (p.Val247Ile)
NM_024649.5(BBS1):c.794C>A (p.Ala265Glu) rs372939761
NM_024649.5(BBS1):c.803G>A (p.Arg268His) rs375949076
NM_024649.5(BBS1):c.830+12C>T rs781283997
NM_024649.5(BBS1):c.831-5C>T rs56177555
NM_024649.5(BBS1):c.867C>T (p.Ser289=)
NM_024649.5(BBS1):c.877G>A (p.Val293Met) rs769422545
NM_024649.5(BBS1):c.887T>C (p.Ile296Thr) rs145094101
NM_024649.5(BBS1):c.901G>A (p.Val301Ile)
NM_024649.5(BBS1):c.951+58C>T
NM_024649.5(BBS1):c.952G>A (p.Gly318Arg) rs1555048487
NM_024649.5(BBS1):c.981C>T (p.Pro327=) rs142243482

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