rs104894466(C;G)

Oculopharyngeal muscular dystrophy (OPMD)

Is a	genotype
of	rs104894466
Gene	BCL2L2-PABPN1, PABPN1, BCL2L2
Chromosome	14
Position	23,321,504
mentioned	by

Magnitude

5

Repute

Bad

Geno	Mag	Summary
(C;G)	5	Oculopharyngeal muscular dystrophy (OPMD)
(G;G)	0	common in clinvar

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