ClinVar Miner

List of variants reported for SchC6pf-Schulz-Passarge syndrome by Natera, Inc.

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 45
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_025216.3(WNT10A):c.493G>A (p.Gly165Arg) rs77583146 0.00755
NM_025216.3(WNT10A):c.208C>T (p.Arg70Trp) rs146460077 0.00089
NM_025216.3(WNT10A):c.321C>A (p.Cys107Ter) rs121908119 0.00087
NM_025216.3(WNT10A):c.591C>T (p.Ala197=) rs367808568 0.00078
NM_025216.3(WNT10A):c.745G>A (p.Val249Ile) rs770985751 0.00048
NM_025216.3(WNT10A):c.234C>T (p.His78=) rs199802454 0.00025
NM_025216.3(WNT10A):c.487C>T (p.Arg163Trp) rs368280129 0.00019
NM_025216.3(WNT10A):c.534A>G (p.Gln178=) rs746227205 0.00018
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.775C>A (p.Arg259=) rs576855744 0.00014
NM_025216.3(WNT10A):c.427C>T (p.His143Tyr) rs202024965 0.00011
NM_025216.3(WNT10A):c.444G>A (p.Ala148=) rs147145554 0.00010
NM_025216.3(WNT10A):c.429C>T (p.His143=) rs747642854 0.00009
NM_025216.3(WNT10A):c.125A>G (p.Asn42Ser) rs149865858 0.00007
NM_025216.3(WNT10A):c.874A>G (p.Ser292Gly) rs767665930 0.00007
NM_025216.3(WNT10A):c.512G>A (p.Arg171His) rs199737793 0.00006
NM_025216.3(WNT10A):c.205C>T (p.Arg69Trp) rs200487809 0.00005
NM_025216.3(WNT10A):c.1005C>T (p.Asp335=) rs779449131 0.00004
NM_025216.3(WNT10A):c.914G>A (p.Arg305His) rs746769946 0.00003
NM_025216.3(WNT10A):c.376+1G>A rs561503117 0.00002
NM_025216.3(WNT10A):c.382C>T (p.Arg128Ter) rs762739726 0.00002
NM_025216.3(WNT10A):c.660C>T (p.Phe220=) rs765046353 0.00002
NM_025216.3(WNT10A):c.742C>T (p.Arg248Ter) rs886039453 0.00002
NM_025216.3(WNT10A):c.966G>C (p.Pro322=) rs767856988 0.00002
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.519G>T (p.Lys173Asn) rs758023820 0.00001
NM_025216.3(WNT10A):c.695G>A (p.Arg232Gln) rs772154760 0.00001
NM_025216.3(WNT10A):c.831G>T (p.Trp277Cys) rs1234227647 0.00001
NM_025216.3(WNT10A):c.891C>G (p.Ala297=) rs748083299 0.00001
NM_025216.3(WNT10A):c.910A>C (p.Asn304His) rs1434390821 0.00001
NM_025216.3(WNT10A):c.957G>T (p.Ser319=) rs774589067 0.00001
NM_025216.3(WNT10A):c.1003G>A (p.Asp335Asn) rs545956598
NM_025216.3(WNT10A):c.1124T>G (p.Met375Arg) rs773598047
NM_025216.3(WNT10A):c.1146C>T (p.Asn382=) rs759671927
NM_025216.3(WNT10A):c.433G>A (p.Val145Met) rs543063101
NM_025216.3(WNT10A):c.4G>A (p.Gly2Ser) rs533605522
NM_025216.3(WNT10A):c.667C>T (p.Arg223Cys) rs149245953
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.958C>T (p.Pro320Ser) rs1944673587
NM_025216.3(WNT10A):c.987_989dup (p.Arg330dup) rs1416466883

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.