Original source

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

Alleles
G/-|Ancestral: G
Location

Chromosome 8:23041061 (forward strand)|View in location tab

Co-located variant

dbSNP rs199870003 (G/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs150035574

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts.

Variant displays