rs143384

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rs143384 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	20	35,437,976 - 35,437,977	snv	G	A	5UTRS;EXON	-
2.	View more	GRCh37	20	34,025,756 - 34,025,757	snv	G	.	5UTRS;EXON	-
3.	View more	GRCh38	20	35,437,976 - 35,437,977	snv	G	?	5UTRS;EXON	-
4.	View more	GRCh38	20	35,437,976 - 35,437,977	snv	G	G	5UTRS;EXON	-

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