rs148783236

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rs148783236 has 3 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	50,492,819 - 50,492,820	snv	A	G	EXON	-
2.	View more	GRCh38	15	50,492,819 - 50,492,820	snv	A	?	EXON	-
3.	View more	GRCh38	15	50,492,819 - 50,492,820	snv	A	A	EXON	-

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