List of variants in gene GSR reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000637.5(GSR):c.866T>C (p.Val289Ala)	rs151187899	0.00150
NM_000637.5(GSR):c.694G>A (p.Gly232Ser)	rs8190976	0.00069
NM_000637.5(GSR):c.697C>T (p.Arg233Cys)	rs145851500	0.00037
NM_000637.5(GSR):c.878C>G (p.Ser293Cys)	rs762024253	0.00008
NM_000637.5(GSR):c.1334C>T (p.Thr445Met)	rs778165636	0.00006
NM_000637.5(GSR):c.1565G>A (p.Arg522His)	rs758486247	0.00006
NM_000637.5(GSR):c.859G>A (p.Val287Met)	rs750862066	0.00004
NM_000637.5(GSR):c.1261A>G (p.Ile421Val)	rs199709765	0.00003
NM_000637.5(GSR):c.307G>A (p.Val103Met)	rs745404470	0.00001
NM_000637.5(GSR):c.512G>T (p.Arg171Leu)	rs766106295
NM_000637.5(GSR):c.698G>A (p.Arg233His)	rs750234827
NM_000637.5(GSR):c.989T>C (p.Leu330Pro)	rs1563529139

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