List of variants in gene RNASEH2C studied for RNASEH2C-related disorder

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_032193.4(RNASEH2C):c.468G>T (p.Ala156=)	rs61736590	0.00159
NM_032193.4(RNASEH2C):c.216G>A (p.Glu72=)	rs1271586408	0.00001
NM_032193.4(RNASEH2C):c.227C>T (p.Pro76Leu)	rs76091978	0.00001
NM_032193.4(RNASEH2C):c.483dup (p.Pro162fs)	rs1309770134	0.00001
NM_032193.4(RNASEH2C):c.247G>A (p.Val83Met)	rs772757667
NM_032193.4(RNASEH2C):c.321A>G (p.Gln107=)	rs2495309911
NM_032193.4(RNASEH2C):c.349-9C>T	rs535966679
NM_032193.4(RNASEH2C):c.468+8G>C	rs751767695

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