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 4:154586358 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 5 transcripts.

Variant displays