Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.27 (T)
Location

Chromosome 7:97026414 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

7:g.97026414T>C

About this variant

This variant overlaps 3 transcripts and has 3065 sample genotypes.

Variant displays