Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386615795

HGVS name

12:g.57762202C>T

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 358 individual genotypes.

Variation displays