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 12:7691534 (forward strand) | View in location tab

Most severe consequence

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 1 individual genotype.

Variation displays