Original source

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

Alleles
A/-|Ancestral: A
Location

Chromosome 7:101132746 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs72298513

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 1 sample genotype.

Variant displays