List of variants in gene PRKDC reported as benign for not specified

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: 16

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HGVS	dbSNP
NM_006904.6(PRKDC):c.10301T>C (p.Ile3434Thr)	rs7830743
NM_006904.6(PRKDC):c.10376A>G (p.Asn3459Ser)	rs8178228
NM_006904.6(PRKDC):c.1623+6A>G	rs1231202
NM_006904.6(PRKDC):c.16G>T (p.Ala6Ser)	rs8177999
NM_006904.6(PRKDC):c.1814C>G (p.Thr605Ser)	rs8178033
NM_006904.6(PRKDC):c.2083C>T (p.Pro695Ser)	rs8178046
NM_006904.6(PRKDC):c.2934+5G>C	rs8178060
NM_006904.6(PRKDC):c.3212A>G (p.Asn1071Ser)	rs8178070
NM_006904.6(PRKDC):c.4809G>T (p.Gln1603His)	rs8178106
NM_006904.6(PRKDC):c.5088T>G (p.Leu1696=)	rs6992074
NM_006904.6(PRKDC):c.6067T>C (p.Ser2023Pro)	rs56042895
NM_006904.6(PRKDC):c.8578-18G>T	rs4873728
NM_006904.6(PRKDC):c.8695C>T (p.Arg2899Cys)	rs4278157
NM_006904.6(PRKDC):c.9922+13C>T	rs8178217
NM_006904.6(PRKDC):c.999G>A (p.Met333Ile)	rs8178017
NM_006904.7(PRKDC):c.2140-13_2140-11del	rs370706897

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