Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y
Location

Chromosome 7:38976621 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

7:g.38976621T>C

About this variant

This variant overlaps 1 transcript.

Variant displays