C0031099[trait identifier] AND "Genetics Laboratory, Lanzhou Universit - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 15987	NM_000583.4(GC):c.1296T>G (p.Asp432Glu)	GC (D432E +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 308841	NM_000376.3(VDR):c.*1906C>A	VDR	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 308862	NM_000376.3(VDR):c.*461G>T	VDR	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 308868	NM_000376.3(VDR):c.*308C>A	VDR	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 308877	NM_000376.3(VDR):c.1056T>C (p.Ile352=)	VDR	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 1252227	NM_000376.3(VDR):c.1025-49G>T	VDR	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1259287	NM_000376.3(VDR):c.1024+283G>A	VDR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 308887	NM_000376.3(VDR):c.2T>C (p.Met1Thr)	VDR (M1T +1 more)	Single nucleotide variant (missense variant +1 more)	Vitamin D-dependent rickets type II with alopecia +2 more	GBenign

ClinVar