List of variants in gene FASTKD2 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001136193.2(FASTKD2):c.777+18T>C	rs200187845	0.00155
NM_001136193.2(FASTKD2):c.192T>C (p.Phe64=)	rs150457139	0.00029
NM_001136193.2(FASTKD2):c.1693C>T (p.Leu565=)	rs148971447	0.00021
NM_001136193.2(FASTKD2):c.756G>A (p.Gln252=)	rs377619612	0.00019
NM_001136193.2(FASTKD2):c.1255-7T>C	rs757255885	0.00014
NM_001136193.2(FASTKD2):c.207A>G (p.Gln69=)	rs144137525	0.00013
NM_001136193.2(FASTKD2):c.1080T>C (p.Leu360=)	rs376045225	0.00011
NM_001136193.2(FASTKD2):c.2014-18T>C	rs749657627	0.00010
NM_001136193.2(FASTKD2):c.2124C>T (p.Ser708=)	rs200616436	0.00007
NM_001136193.2(FASTKD2):c.1115-10A>G	rs747618392	0.00006
NM_001136193.2(FASTKD2):c.1698G>A (p.Pro566=)	rs151258385	0.00002
NM_001136193.2(FASTKD2):c.1427+20dup	rs371981683
NM_001136193.2(FASTKD2):c.2014-12_2014-11del	rs770341016

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