List of variants in gene WDR35 studied for connective tissue disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_020779.4(WDR35):c.3019C>T (p.Arg1007Cys)	rs56395266	0.01130
NM_020779.4(WDR35):c.3279G>C (p.Gln1093His)	rs148436608	0.00161
NM_020779.4(WDR35):c.1183A>T (p.Asn395Tyr)	rs143343508	0.00135
NM_020779.4(WDR35):c.770T>C (p.Val257Ala)	rs142955097	0.00095
NM_020779.4(WDR35):c.853A>T (p.Ile285Phe)	rs200059077	0.00073
NM_020779.4(WDR35):c.765C>T (p.Tyr255=)	rs117255034	0.00013
NM_001006657.2(WDR35):c.1215A>G (p.Thr405=)	rs144673252	0.00011
NM_020779.4(WDR35):c.2593G>A (p.Val865Met)	rs1032877870	0.00001
NM_020779.4(WDR35):c.761T>C (p.Met254Thr)	rs547986777	0.00001
NM_020779.4(WDR35):c.1255+5G>A	rs1034087679
NM_020779.4(WDR35):c.1833C>G (p.Asn611Lys)	rs1671026684
NM_020779.4(WDR35):c.2409A>G (p.Gln803=)	rs140630290
NM_020779.4(WDR35):c.658G>A (p.Val220Met)	rs746602378

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