Original source

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

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

Chromosome 16:47665985 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 262 sample genotypes.

Variant displays