Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.28 (A)
Location

Chromosome 13:75589660 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17064748, rs12877452

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2700 individual genotypes.

Variation displays