Original source

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

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

Chromosome 7:103485253 (forward strand)|View in location tab

Co-located variant

dbSNP rs35324403 (A/-)

Most severe consequence
 
Intron variant
HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts.

Variant displays