Original source

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

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

Chromosome 12:52469293 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1132961

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2 individual genotypes.

Variation displays