List of variants in gene MED13L reported by Neuberg Centre For Genomic Medicine, NCGM

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_015335.5(MED13L):c.1136G>A (p.Arg379Gln)	rs758022508	0.00002
NM_015335.5(MED13L):c.1802T>C (p.Leu601Pro)	rs2499911829
NM_015335.5(MED13L):c.2114C>G (p.Pro705Arg)	rs2137378723
NM_015335.5(MED13L):c.2227A>C (p.Lys743Gln)	rs2499905849
NM_015335.5(MED13L):c.2779G>A (p.Glu927Lys)
NM_015335.5(MED13L):c.3278A>G (p.Asn1093Ser)
NM_015335.5(MED13L):c.47A>G (p.Asp16Gly)	rs2500191290
NM_015335.5(MED13L):c.5273G>C (p.Cys1758Ser)
NM_015335.5(MED13L):c.5904G>A (p.Met1968Ile)	rs2137223825
NM_015335.5(MED13L):c.6041A>G (p.Asn2014Ser)

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