Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.16 (A)
Location

Chromosome 7:44146289 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2506 sample genotypes and is mentioned in 1 citation.

Variant displays