Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M
Location

Chromosome 7:94628075 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17324450

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 72 sample genotypes.

Variant displays