Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.15 (C)
Location

Chromosome 7:97020044 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms
HGVS name

7:g.97020044A>C

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 3 transcripts and has 6005 sample genotypes.

Variant displays