Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

-/AC | MAF: 0.03 (-)

Chromosome 16: between 74756895 and 74756896 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs149741683

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2514 sample genotypes.

Variant displays