Original source

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

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2508 sample genotypes.

Variant displays