Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 1:17005754 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM071562

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_058451

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 10 transcripts.

Variant displays