Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.03 (A)
Location

Chromosome 3:165772869 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

3:g.165772869C>A

About this variant

This variant overlaps 4 transcripts and has 2504 sample genotypes.

Variant displays