ClinVar Miner

List of variants reported as uncertain significance for SchC6pf-Schulz-Passarge syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_025216.3(WNT10A):c.493G>A (p.Gly165Arg) rs77583146 0.00755
NM_025216.3(WNT10A):c.-123C>A rs928677784 0.00067
NM_025216.3(WNT10A):c.1087A>C (p.Asn363His) rs34972707 0.00062
NM_025216.3(WNT10A):c.*108G>A rs190527122 0.00040
NM_025216.2(WNT10A):c.-341A>G rs762914440 0.00029
NM_025216.3(WNT10A):c.756+14C>T rs200733269 0.00029
NM_025216.3(WNT10A):c.668G>A (p.Arg223His) rs143424659 0.00028
NM_025216.2(WNT10A):c.-149G>T rs886055641 0.00022
NM_025216.3(WNT10A):c.487C>T (p.Arg163Trp) rs368280129 0.00019
NM_025216.3(WNT10A):c.1017C>T (p.Phe339=) rs531326479 0.00016
NM_025216.3(WNT10A):c.216G>T (p.Met72Ile) rs373607885 0.00016
NM_025216.3(WNT10A):c.149C>T (p.Pro50Leu) rs199980023 0.00011
NM_025216.3(WNT10A):c.347T>C (p.Ile116Thr) rs762311530 0.00011
NM_025216.3(WNT10A):c.427C>T (p.His143Tyr) rs202024965 0.00011
NM_025216.2(WNT10A):c.-270G>C rs774035749 0.00010
NM_025216.3(WNT10A):c.444G>A (p.Ala148=) rs147145554 0.00010
NM_025216.3(WNT10A):c.205C>T (p.Arg69Trp) rs200487809 0.00005
NM_025216.3(WNT10A):c.551G>A (p.Arg184His) rs372756514 0.00005
NM_025216.3(WNT10A):c.1134C>T (p.Gly378=) rs886055644 0.00004
NM_025216.3(WNT10A):c.349C>T (p.Pro117Ser) rs144212422 0.00004
NM_025216.3(WNT10A):c.437C>G (p.Ser146Cys) rs759718991 0.00004
NM_025216.3(WNT10A):c.498C>T (p.Asp166=) rs143463683 0.00004
NM_025216.3(WNT10A):c.*115C>T rs886055646 0.00003
NM_025216.3(WNT10A):c.914G>A (p.Arg305His) rs746769946 0.00003
NM_025216.2(WNT10A):c.-285C>T rs886055636 0.00002
NM_025216.3(WNT10A):c.*15C>T rs886055645 0.00002
NM_025216.3(WNT10A):c.377-11T>C rs369995297 0.00002
NM_025216.3(WNT10A):c.660C>T (p.Phe220=) rs765046353 0.00002
NM_025216.3(WNT10A):c.694C>T (p.Arg232Trp) rs193098360 0.00002
NM_025216.2(WNT10A):c.-153G>A rs886055640 0.00001
NM_025216.3(WNT10A):c.*238C>T rs1176499706 0.00001
NM_025216.3(WNT10A):c.-70G>C rs1042922024 0.00001
NM_025216.3(WNT10A):c.1061C>T (p.Ser354Leu) rs781178898 0.00001
NM_025216.3(WNT10A):c.1162C>T (p.Arg388Cys) rs1186983054 0.00001
NM_025216.3(WNT10A):c.283G>A (p.Glu95Lys) rs318240759 0.00001
NM_025216.3(WNT10A):c.403G>A (p.Ala135Thr) rs1402990329 0.00001
NM_025216.3(WNT10A):c.443C>T (p.Ala148Val) rs373695499 0.00001
NM_025216.3(WNT10A):c.519G>T (p.Lys173Asn) rs758023820 0.00001
NM_025216.3(WNT10A):c.526C>T (p.Arg176Cys) rs754010310 0.00001
NM_025216.3(WNT10A):c.652A>G (p.Met218Val) rs373991357 0.00001
NM_025216.3(WNT10A):c.695G>A (p.Arg232Gln) rs772154760 0.00001
NM_025216.3(WNT10A):c.697G>A (p.Glu233Lys) rs121908118 0.00001
NM_025216.3(WNT10A):c.831G>T (p.Trp277Cys) rs1234227647 0.00001
NM_025216.3(WNT10A):c.838A>T (p.Thr280Ser) rs886055643 0.00001
NM_025216.3(WNT10A):c.910A>C (p.Asn304His) rs1434390821 0.00001
NM_025216.2(WNT10A):c.-194dup rs886055639
NM_025216.2(WNT10A):c.-202G>C rs886055638
NM_025216.2(WNT10A):c.-249G>C rs571829301
NM_025216.2(WNT10A):c.-358G>A rs886055635
NM_025216.2(WNT10A):c.-370C>A rs886055634
NM_025216.2(WNT10A):c.-433C>G rs886055633
NM_025216.3(WNT10A):c.*139C>G rs1944681589
NM_025216.3(WNT10A):c.*339C>T rs1944683536
NM_025216.3(WNT10A):c.*441C>T rs886055647
NM_025216.3(WNT10A):c.1035C>A (p.Phe345Leu) rs1944675395
NM_025216.3(WNT10A):c.1049C>T (p.Pro350Leu) rs564146190
NM_025216.3(WNT10A):c.1124T>G (p.Met375Arg) rs773598047
NM_025216.3(WNT10A):c.166A>G (p.Asn56Asp) rs992196031
NM_025216.3(WNT10A):c.315G>C (p.Trp105Cys) rs886055642
NM_025216.3(WNT10A):c.364A>T (p.Ile122Phe) rs201929547
NM_025216.3(WNT10A):c.433G>A (p.Val145Met) rs543063101
NM_025216.3(WNT10A):c.483G>C (p.Ala161=) rs200751156
NM_025216.3(WNT10A):c.653T>G (p.Met218Arg) rs759559158
NM_025216.3(WNT10A):c.664G>A (p.Glu222Lys) rs377416834
NM_025216.3(WNT10A):c.667C>T (p.Arg223Cys) rs149245953
NM_025216.3(WNT10A):c.719C>T (p.Ala240Val) rs201578578
NM_025216.3(WNT10A):c.756+13C>A rs745958462
NM_025216.3(WNT10A):c.796G>A (p.Gly266Ser) rs778752861
NM_025216.3(WNT10A):c.801G>A (p.Thr267=) rs553058408
NM_025216.3(WNT10A):c.841C>A (p.Pro281Thr) rs541715493
NM_025216.3(WNT10A):c.841C>G (p.Pro281Ala) rs541715493
NM_025216.3(WNT10A):c.958C>T (p.Pro320Ser) rs1944673587
NM_025216.3(WNT10A):c.987_989dup (p.Arg330dup) rs1416466883

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