Related gene-specific medical variations for Gene (Select 6241) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2343224	NR_164157.1(RRM2):n.1182A>T	C2orf48, RRM2 (M26L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2259439	NM_182626.2:c.145T>C	C2orf48, RRM2	Single nucleotide variant	not specified	GUncertain significance
Select item 2223871	NR_164157.1(RRM2):n.1554C>A	C2orf48, RRM2	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance

Format

Sort by

Choose Destination