Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.26 (A)
Location

Chromosome 17:27765235 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59865181

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

About this variant

This variant overlaps 2 transcripts and has 2596 individual genotypes.

Variation displays