Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17324450

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 72 individual genotypes.

Variation displays