2 variants found for this position

Variant	RHeference identifier	Allele	Category
single nucleotide polyphormism -> missense	RHef00234	RHD*364A,602G,667G,744T,1025C (weak D type 4.2.3(S122T))	missense
single nucleotide polyphormism -> missense	RHef00642	RHD*186T,364A,873A	missense