Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 6:43515193 (forward strand) | View in location tab

Most severe consequence

This variation has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 28 transcripts and has 1 individual genotype.

Variation displays