rs2993481

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rs2993481 has 4 RGD Records - Homo sapiens

Page 1 of 1

	Variant Page	Assembly	Chr	Position	Type	Reference Nucleotide	Variant Nucleotide	Location Name	Is Damaging?
1.	View more	GRCh38	1	3,056,869 - 3,056,870	snv	A	T	3UTRS;EXON;INTRON	-
2.	View more	GRCh38	1	3,056,869 - 3,056,870	snv	A	T	3UTRS;EXON;INTRON	-
3.	View more	GRCh38	1	3,056,869 - 3,056,870	snv	A	A	3UTRS;EXON;INTRON	-
4.	View more	GRCh38	1	3,056,869 - 3,056,870	snv	A	?	3UTRS;EXON;INTRON	-

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.