NM_000439.4(PCSK1):c.661A>G (p.Asn221Asp) | -1 | - | risk factor | 6232 | RCV000022673; | N | MedGen:C2676498,OMIM:612362 | 5 | 95751785 | 95751785 | NM_000439.4:c.661A>G | NP_000430.3:p.Asn221Asp | NC_000005.9:g.95751785T>C | OMIM Allelic Variant:162150.0005 | C2676498 612362 Body mass index quantitative trait locus 12 | | |