ClinVar Miner

List of variants in gene CHD7 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP
NM_017780.3(CHD7):c.*1495C>T rs139790301
NM_017780.3(CHD7):c.*1502G>A rs181017286
NM_017780.3(CHD7):c.*1579A>G rs10100774
NM_017780.3(CHD7):c.*2104T>A rs16926520
NM_017780.3(CHD7):c.*96C>A rs193154029
NM_017780.3(CHD7):c.-380C>T rs113958504
NM_017780.3(CHD7):c.1018A>G (p.Met340Val) rs41305525
NM_017780.3(CHD7):c.1281T>C (p.Tyr427=) rs373942842
NM_017780.3(CHD7):c.1419G>C (p.Gly473=) rs186394299
NM_017780.3(CHD7):c.1565G>T (p.Gly522Val) rs142962579
NM_017780.3(CHD7):c.1737G>A (p.Gln579=) rs747922099
NM_017780.3(CHD7):c.2053_2058dupGCAAAA (p.Lys686_Thr687insAlaLys) rs377139749
NM_017780.3(CHD7):c.2067G>A (p.Thr689=) rs34979623
NM_017780.3(CHD7):c.2124T>C (p.Ser708=) rs79302359
NM_017780.3(CHD7):c.216T>C (p.Tyr72=) rs16926453
NM_017780.3(CHD7):c.2457G>A (p.Glu819=) rs1060504849
NM_017780.3(CHD7):c.2498+12G>T rs557099951
NM_017780.3(CHD7):c.2614-7G>T rs762399977
NM_017780.3(CHD7):c.2680A>G (p.Thr894Ala) rs377662366
NM_017780.3(CHD7):c.2751G>A (p.Thr917=) rs369429961
NM_017780.3(CHD7):c.2831G>A (p.Arg944His) rs117506164
NM_017780.3(CHD7):c.2835+8T>C rs202141372
NM_017780.3(CHD7):c.307T>A (p.Ser103Thr) rs41272435
NM_017780.3(CHD7):c.3241A>G (p.Ile1081Val) rs768184220
NM_017780.3(CHD7):c.4089C>G (p.Leu1363=) rs974334602
NM_017780.3(CHD7):c.4534-13T>G rs114996731
NM_017780.3(CHD7):c.4851T>G (p.Gly1617=) rs181927766
NM_017780.3(CHD7):c.5051-4C>T rs71640288
NM_017780.3(CHD7):c.5172G>A (p.Glu1724=) rs1554602576
NM_017780.3(CHD7):c.5271G>A (p.Ala1757=) rs775003129
NM_017780.3(CHD7):c.5307C>T (p.Ala1769=) rs16926499
NM_017780.3(CHD7):c.5697C>G (p.Gly1899=) rs528130317
NM_017780.3(CHD7):c.5754T>C (p.Thr1918=) rs61746542
NM_017780.3(CHD7):c.6080G>A (p.Arg2027Gln) rs372077201
NM_017780.3(CHD7):c.6111C>T (p.Pro2037=) rs41312170
NM_017780.3(CHD7):c.6135G>A (p.Pro2045=) rs6999971
NM_017780.3(CHD7):c.6282A>G (p.Gly2094=) rs41312172
NM_017780.3(CHD7):c.6353A>G (p.Asn2118Ser) rs199614124
NM_017780.3(CHD7):c.6478G>A (p.Ala2160Thr) rs61753399
NM_017780.3(CHD7):c.6513C>T (p.Ala2171=) rs376020564
NM_017780.3(CHD7):c.657C>T (p.Gly219=) rs113483301
NM_017780.3(CHD7):c.6669C>T (p.Val2223=) rs556577614
NM_017780.3(CHD7):c.6738G>A (p.Glu2246=) rs61729627
NM_017780.3(CHD7):c.6924G>A (p.Ser2308=) rs61733338
NM_017780.3(CHD7):c.694C>A (p.Pro232Thr) rs554647169
NM_017780.3(CHD7):c.6989_6990delGCinsCT (p.Gly2330Ala) rs1554604771
NM_017780.3(CHD7):c.7059A>G (p.Thr2353=) rs1271940749
NM_017780.3(CHD7):c.7086C>T (p.Ser2362=) rs757280832
NM_017780.3(CHD7):c.7209G>A (p.Arg2403=) rs61746518
NM_017780.3(CHD7):c.7278G>A (p.Gln2426=) rs187311127
NM_017780.3(CHD7):c.7356A>G (p.Thr2452=) rs2272727
NM_017780.3(CHD7):c.7570C>T (p.Leu2524=) rs751931671
NM_017780.3(CHD7):c.7579A>C (p.Met2527Leu) rs192129249
NM_017780.3(CHD7):c.7972-10C>G rs912810188
NM_017780.3(CHD7):c.8034A>G (p.Glu2678=) rs559053565
NM_017780.3(CHD7):c.8047C>T (p.Pro2683Ser) rs201319489
NM_017780.3(CHD7):c.8199T>C (p.Ala2733=) rs878855033
NM_017780.3(CHD7):c.8416C>G (p.Leu2806Val) rs45521933
NM_017780.3(CHD7):c.8478C>T (p.Asn2826=) rs202076455
NM_017780.3(CHD7):c.8580C>T (p.Ser2860=) rs767368987
NM_017780.3(CHD7):c.8740G>A (p.Gly2914Arg) rs187751757
NM_017780.3(CHD7):c.8919C>T (p.Asp2973=) rs368038649
NM_017780.3(CHD7):c.8950C>T (p.Leu2984Phe) rs184814820

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