"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "SIGLEC16"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2650294	NM_001348364.2(SIGLEC16):c.421-6C>T	SIGLEC16	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2650295	NR_002825.2(SIGLEC16):n.673G>A	SIGLEC16 (R192K)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2650296	NR_002825.2(SIGLEC16):n.710G>A	SIGLEC16	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2650297	NR_002825.2(SIGLEC16):n.837C>T	SIGLEC16	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2650298	NR_002825.2(SIGLEC16):n.902G>A	SIGLEC16	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2650299	NR_002825.2(SIGLEC16):n.960A>C	SIGLEC16 (T288P)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

ClinVar