Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.25 (C)
Location

Chromosome 16:57370858 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

16:g.57370858C>T

About this variant

This variant overlaps 4 transcripts and has 2509 sample genotypes.

Variant displays