ClinVar Miner

List of variants in gene ZDHHC9 reported as benign for X-linked disease

Included ClinVar conditions (274):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_016032.4(ZDHHC9):c.487+15A>G rs2275605 0.92100
NM_016032.4(ZDHHC9):c.-204+6G>T rs3747339 0.00480
NM_016032.4(ZDHHC9):c.975C>T (p.Ser325=) rs139619000 0.00414
NM_016032.4(ZDHHC9):c.167+10G>A rs140526450 0.00244
NM_016032.4(ZDHHC9):c.777+16C>T rs193236859 0.00196
NM_016032.4(ZDHHC9):c.626-10A>T rs188156112 0.00103
NM_016032.4(ZDHHC9):c.291G>A (p.Ala97=) rs77513704 0.00035
NM_016032.4(ZDHHC9):c.978+15C>T rs367975001 0.00022
NM_016032.4(ZDHHC9):c.984C>G (p.Pro328=) rs146317883 0.00010
NM_016032.4(ZDHHC9):c.144A>T (p.Thr48=) rs145877196 0.00009
NM_016032.4(ZDHHC9):c.674+9C>T rs376385410 0.00009
NM_016032.4(ZDHHC9):c.1033G>A (p.Glu345Lys) rs185917523 0.00008
NM_016032.4(ZDHHC9):c.168-18A>G rs753763200 0.00008
NM_016032.4(ZDHHC9):c.369G>A (p.Pro123=) rs763192908 0.00004
NM_016032.4(ZDHHC9):c.674+20T>C rs45555436 0.00004
NM_016032.4(ZDHHC9):c.1014G>A (p.Pro338=) rs774643586 0.00003
NM_016032.4(ZDHHC9):c.1032C>T (p.Pro344=) rs755391148 0.00003
NM_016032.4(ZDHHC9):c.167+9C>T rs746318308 0.00003
NM_016032.4(ZDHHC9):c.674+11C>T rs370687569 0.00002
NM_016032.4(ZDHHC9):c.487+17G>A rs572453121 0.00001
NM_016032.4(ZDHHC9):c.979-18A>G rs202246689 0.00001
NM_016032.4(ZDHHC9):c.354G>C (p.Gln118His) rs1927947896
NM_016032.4(ZDHHC9):c.488-15C>G
NM_016032.4(ZDHHC9):c.488-19CT[3] rs762762877
NM_016032.4(ZDHHC9):c.621C>T (p.Ala207=)
NM_016032.4(ZDHHC9):c.674+10G>A
NM_016032.4(ZDHHC9):c.714C>T (p.Ser238=)
NM_016032.4(ZDHHC9):c.987A>C (p.Thr329=)

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