Original source

Variants (including SNPs and indels) imported from dbSNP (release 136) | View in dbSNP

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

Chromosome 19:13575517 (forward strand) | View in location tab

Most severe consequence
Missense variant

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

About this variant

This variant overlaps 1 transcript.

Variant displays