rs3848519(C;C)

common in complete genomics

Is a	genotype
of	rs3848519
Gene	FECH
Chromosome	18
Position	57,580,104
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;A)	1	likely to be a benign variant
(A;C)	1	likely to be a benign variant
(C;C)	0	common in complete genomics