Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/A | MAF: 0.17 (A)
Location

Chromosome 16: between 74760600 and 74760601 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs79559612, rs148998226

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2509 individual genotypes.

Variation displays