rs104893666(C;C)

common in clinvar

Is a	genotype
of	rs104893666
Gene	SPR
Chromosome	2
Position	72,888,497
mentioned	by

Magnitude

0

Repute

Good

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