Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 11:102775613 (forward strand) | View in location tab

Most severe consequence

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

About this variant

This variant overlaps 3 transcripts and has 36 individual genotypes.

Variation displays