Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

Chromosome 5:161873225 (forward strand) | View in location tab

Most severe consequence
Missense variant
HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 262 sample genotypes.

Variant displays