Original source

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