"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "RNU7-1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1711335	NM_138425.3(C12orf57):c.-276G>C	C12orf57, RNU7-1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1202612	NM_138425.3(C12orf57):c.-267_-260delCTGGCTTT	C12orf57, RNU7-1	Deletion (non-coding transcript variant +1 more)	not provided	GLikely pathogenic
Select item 1301230	NM_138425.3(C12orf57):c.-271C>T	C12orf57, RNU7-1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign/Likely benign
Select item 1711336	NM_138425.3(C12orf57):c.-270T>G	C12orf57, RNU7-1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2578675	NM_138425.3(C12orf57):c.-266T>C	C12orf57, RNU7-1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 3024660	NM_138425.3(C12orf57):c.-258T>C	C12orf57, RNU7-1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1202613	NM_138425.3(C12orf57):c.-256C>T	C12orf57, RNU7-1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign/Likely benign

ClinVar