List of variants in gene SRRT reported by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_015908.6(SRRT):c.795T>C (p.Leu265=)	rs15624	0.52205
NM_015908.6(SRRT):c.1042-18C>G	rs6942607	0.51325
NM_015908.6(SRRT):c.1042-7C>T	rs3757866	0.01309
NM_015908.6(SRRT):c.615G>A (p.Glu205=)	rs145327657	0.00632
NM_015908.6(SRRT):c.2556-9A>T	rs150287642	0.00402
NM_015908.6(SRRT):c.471C>T (p.Leu157=)	rs143241109	0.00394
NM_015908.6(SRRT):c.1554C>G (p.Arg518=)	rs149979693	0.00363

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