Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.28 (T)
Location

Chromosome 6:52450521 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2508 individual genotypes.

Variation displays