Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.31 (A)
Location

Chromosome 7:2374915 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs10350324

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2508 sample genotypes.

Variant displays