Original source

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

Alleles
C/-|Ancestral: C
Location

Chromosome 16:31178121 (forward strand)|View in location tab

Co-located variant

dbSNP rs12051357 (C/A/T)

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 9 transcripts.

Variant displays