rs633695

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rs633695 has 5 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	15	58,433,640 - 58,433,641	snv	A	T	INTRON	-
2.	View more	GRCh38	15	58,433,640 - 58,433,641	snv	A	C	INTRON	-
3.	View more	GRCh38	15	58,433,640 - 58,433,641	snv	A	G	INTRON	-
4.	View more	GRCh38	15	58,433,640 - 58,433,641	snv	A	?	INTRON	-
5.	View more	GRCh38	15	58,433,640 - 58,433,641	snv	A	A	INTRON	-

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