List of variants in gene ASRGL1 reported as benign for not provided

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_001083926.2(ASRGL1):c.495C>T (p.Asn165=)	rs3741244	0.00528
NM_001083926.2(ASRGL1):c.97G>A (p.Val33Met)	rs115409110	0.00502
NM_001083926.2(ASRGL1):c.375T>C (p.Phe125=)	rs75102382	0.00249
NM_001083926.2(ASRGL1):c.798C>T (p.Ile266=)	rs151164229	0.00173
NM_001083926.2(ASRGL1):c.24C>T (p.His8=)	rs143657589	0.00151
NM_001083926.2(ASRGL1):c.867G>A (p.Lys289=)	rs145379105	0.00149
NM_001083926.2(ASRGL1):c.627C>T (p.Ala209=)	rs147442110	0.00067
NM_001083926.2(ASRGL1):c.162C>T (p.Ala54=)	rs142016448	0.00026
NM_001083926.2(ASRGL1):c.191-14_191-12del	rs558946011
NM_001083926.2(ASRGL1):c.334-14dup
NM_001083926.2(ASRGL1):c.722-4del	rs1947352544
NM_001083926.2(ASRGL1):c.753G>A (p.Ser251=)	rs149188142

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