Original source

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

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

Chromosome 1:16990147 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts.

Variant displays