List of variants in gene combination RHD, RSRP1 reported by Australian Red Cross Blood Service

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_016124.6(RHD):c.1063G>A (p.Gly355Ser)	rs146093871	0.00056
NM_016124.6(RHD):c.270G>C (p.Trp90Cys)	rs1248638537
NM_016124.6(RHD):c.277_278delinsGG (p.Leu93Gly)	rs2124622201
NM_016124.6(RHD):c.341G>C (p.Arg114Pro)	rs530929152
NM_016124.6(RHD):c.452G>A (p.Gly151Asp)	rs879255550
NM_016124.6(RHD):c.709G>A (p.Ala237Thr)	rs2124675598
NM_016124.6(RHD):c.[186G>T;410C>T455A>C602C>G604G>A733G>C]

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