rs104893665(A;A)

common in clinvar

Is a	genotype
of	rs104893665
Gene	SPR
Chromosome	2
Position	72,888,457
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	3	Carrier of a SPR deficiency mutation