List of variants in gene WNT10A reported as likely pathogenic for diffuse palmoplantar keratoderma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_025216.3(WNT10A):c.383G>A (p.Arg128Gln)	rs121908121	0.00007
NM_025216.3(WNT10A):c.391G>A (p.Ala131Thr)	rs372993798	0.00004
NM_025216.3(WNT10A):c.382C>T (p.Arg128Ter)	rs762739726	0.00002
NM_025216.3(WNT10A):c.1028C>T (p.Pro343Leu)	rs1944675271	0.00001
NM_025216.3(WNT10A):c.310C>T (p.Arg104Cys)	rs764658964	0.00001
NM_025216.3(WNT10A):c.-17_13del (p.Met1_His5del)	rs746813123
NM_025216.3(WNT10A):c.1066G>A (p.Gly356Ser)
NM_025216.3(WNT10A):c.1079G>C (p.Arg360Pro)	rs893127185
NM_025216.3(WNT10A):c.113+1G>A
NM_025216.3(WNT10A):c.274G>A (p.Ala92Thr)
NM_025216.3(WNT10A):c.318C>G (p.Asn106Lys)	rs1283426045
NM_025216.3(WNT10A):c.322T>C (p.Ser108Pro)	rs1249944381
NM_025216.3(WNT10A):c.3G>A (p.Met1Ile)
NM_025216.3(WNT10A):c.433G>A (p.Val145Met)	rs543063101
NM_025216.3(WNT10A):c.521T>C (p.Leu174Pro)
NM_025216.3(WNT10A):c.616C>T (p.Gln206Ter)	rs1060499588
NM_025216.3(WNT10A):c.662G>T (p.Gly221Val)
NM_025216.3(WNT10A):c.694del (p.Arg232fs)	rs1575233692
NM_025216.3(WNT10A):c.814C>T (p.Gln272Ter)	rs773036759
NM_025216.3(WNT10A):c.949del (p.Ala317fs)	rs775990266

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