Original source

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

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

Chromosome 12:57762202 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs386615795

HGVS name

12:g.57762202C>T

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 10 transcripts and has 358 sample genotypes.

Variant displays